Canonical Allele Identifier: CA392000343

Gene: CAPN3

Linked Data

• ClinVar Variation Id: 1256093
• ClinVar RCV Id: RCV001663435
• dbSNP Id: rs2141203159
• MyVariant Identifiers: chr15:g.42695119T>A (hg19) ; chr15:g.42402921T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42402921T>A , CM000677.2:g.42402921T>A	GRCh38
NC_000015.9:g.42695119T>A , CM000677.1:g.42695119T>A	GRCh37
NC_000015.8:g.40482411T>A	NCBI36
NG_008660.1:g.59819T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349748.8:c.1520T>A	ENSP00000183936.4:p.Val507Asp
ENST00000357568.8:c.1664T>A	ENSP00000350181.3:p.Val555Asp
ENST00000397163.8:c.1664T>A MANE Select	ENSP00000380349.3:p.Val555Asp
ENST00000466369.5:n.2173T>A
ENST00000483208.5:n.2553T>A
ENST00000495723.1:n.2553T>A
ENST00000549793.5:n.1895T>A
ENST00000638141.2:n.1535T>A
ENST00000673646.1:c.128T>A	ENSP00000501007.1:p.Val43Asp
ENST00000673705.1:c.309+3269T>A	ENSP00000501021.1:n.309+3269T>A
ENST00000673813.1:n.580+6T>A
ENST00000318023.11:c.1520T>A	ENSP00000326281.8:p.Val507Asp
ENST00000349748.7:c.1520T>A	ENSP00000183936.4:p.Val507Asp
ENST00000357568.7:c.1664T>A	ENSP00000350181.3:p.Val555Asp
ENST00000397163.7:c.1664T>A	ENSP00000380349.3:p.Val555Asp
ENST00000397200.8:c.128T>A	ENSP00000380384.4:p.Val43Asp
ENST00000567071.5:c.123T>A
ENST00000569827.5:c.128T>A	ENSP00000454379.1:p.Val43Asp
NM_000070.2:c.1664T>A	NP_000061.1:p.Val555Asp
NM_024344.1:c.1664T>A	NP_077320.1:p.Val555Asp
NM_173087.1:c.1520T>A	NP_775110.1:p.Val507Asp
NM_173088.1:c.128T>A	NP_775111.1:p.Val43Asp
NM_000070.3:c.1664T>A MANE Select	NP_000061.1:p.Val555Asp
NM_024344.2:c.1664T>A	NP_077320.1:p.Val555Asp
NM_173087.2:c.1520T>A	NP_775110.1:p.Val507Asp
NM_173088.2:c.128T>A	NP_775111.1:p.Val43Asp