Variant position: 101 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: 377 The length of the canonical sequence.
Location on the sequence:
The residue change on the sequence. Unless the variant is located at the beginning or at the end of the protein sequence, both residues upstream (20) and downstream (20) of the variant will be shown.
Residue conservation: The multiple alignment of the region surrounding the variant against various orthologous sequences.
Human WDDMEKIWHHTFYNELRVAP EEHPTLLTEAPLNPKANREKM
Mouse WDDMEKIWHHTFYNELRVAP EEHPTLLTEAPLNPKANREKM
Rat WDDMEKIWHHTFYNELRVAP EEHPTLLTEAPLNPKANREKM
Bovine WDDMEKIWHHTFYNELRVAP EEHPTLLTEAPLNPKANREKM
Chicken WDDMEKIWHHTFYNELRVAP EEHPTLLTEAPLNPKANREKM
Xenopus laevis WDDMEKIWHHTFYNELRVAP EEHPTLLTEAPLNPKANREKM
Xenopus tropicalis WDDMEKIWHHTFYNELRVAP EEHPTLLTEAPLNPKANREKM
Sequence annotation in neighborhood: The regions or sites of interest surrounding the variant. In general the features listed are posttranslational modifications, binding sites, enzyme active sites, local secondary structure or other characteristics reported in the cited references. The "Sequence annotation in neighborhood" lines have a fixed format:
Type: the type of sequence feature. Positions: endpoints of the sequence feature. Description: contains additional information about the feature.
Type Positions Description
2 – 377 Actin, alpha cardiac muscle 1, intermediate form
3 – 377 Actin, alpha cardiac muscle 1
86 – 86 N6-methyllysine
Inherited and de novo mutations in the cardiac actin gene cause hypertrophic cardiomyopathy.
Olson T.M.; Doan T.P.; Kishimoto N.Y.; Whitby F.G.; Ackerman M.J.; Fananapazir L.;
J. Mol. Cell. Cardiol. 32:1687-1694(2000)
Cited for: VARIANTS CMH11 LYS-101; ALA-166 AND PRO-333;
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