Canonical Allele Identifier: CA391999860

Gene: CAPN3

Linked Data

• ClinVar Variation Id: 595476
• ClinVar RCV Id: RCV000731030
• dbSNP Id: rs1566980383
• MyVariant Identifiers: chr15:g.42693928G>A (hg19) ; chr15:g.42401730G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42401730G>A , CM000677.2:g.42401730G>A	GRCh38
NC_000015.9:g.42693928G>A , CM000677.1:g.42693928G>A	GRCh37
NC_000015.8:g.40481220G>A	NCBI36
NG_008660.1:g.58628G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349748.8:c.1300G>A	ENSP00000183936.4:p.Val434Met
ENST00000357568.8:c.1444G>A	ENSP00000350181.3:p.Val482Met
ENST00000397163.8:c.1444G>A MANE Select	ENSP00000380349.3:p.Val482Met
ENST00000466369.5:n.1953G>A
ENST00000483208.5:n.1675G>A
ENST00000495723.1:n.1675G>A
ENST00000549793.5:n.1675G>A
ENST00000638141.2:n.1315G>A
ENST00000673705.1:c.309+2078G>A	ENSP00000501021.1:n.309+2078G>A
ENST00000318023.11:c.1300G>A	ENSP00000326281.8:p.Val434Met
ENST00000349748.7:c.1300G>A	ENSP00000183936.4:p.Val434Met
ENST00000357568.7:c.1444G>A	ENSP00000350181.3:p.Val482Met
ENST00000397163.7:c.1444G>A	ENSP00000380349.3:p.Val482Met
NM_000070.2:c.1444G>A	NP_000061.1:p.Val482Met
NM_024344.1:c.1444G>A	NP_077320.1:p.Val482Met
NM_173087.1:c.1300G>A	NP_775110.1:p.Val434Met
NM_000070.3:c.1444G>A MANE Select	NP_000061.1:p.Val482Met
NM_024344.2:c.1444G>A	NP_077320.1:p.Val482Met
NM_173087.2:c.1300G>A	NP_775110.1:p.Val434Met