Canonical Allele Identifier: CA618001513

Gene: CAPN3

Linked Data

• dbSNP Id: rs1455492901
• gnomAD v2: 15-42693831-G-A
• gnomAD v4: 15-42401633-G-A
• MyVariant Identifiers: chr15:g.42693831G>A (hg19) ; chr15:g.42401633G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42401633G>A , CM000677.2:g.42401633G>A	GRCh38
NC_000015.9:g.42693831G>A , CM000677.1:g.42693831G>A	GRCh37
NC_000015.8:g.40481123G>A	NCBI36
NG_008660.1:g.58531G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349748.8:c.1211-8G>A	ENSP00000183936.4:n.1211-8G>A
ENST00000357568.8:c.1355-8G>A	ENSP00000350181.3:n.1355-8G>A
ENST00000397163.8:c.1355-8G>A MANE Select	ENSP00000380349.3:n.1355-8G>A
ENST00000466369.5:n.1864-8G>A
ENST00000483208.5:n.1586-8G>A
ENST00000495723.1:n.1586-8G>A
ENST00000549793.5:n.1586-8G>A
ENST00000638141.2:n.1226-8G>A
ENST00000673705.1:c.309+1981G>A	ENSP00000501021.1:n.309+1981G>A
ENST00000318023.11:c.1211-8G>A	ENSP00000326281.8:n.1211-8G>A
ENST00000349748.7:c.1211-8G>A	ENSP00000183936.4:n.1211-8G>A
ENST00000357568.7:c.1355-8G>A	ENSP00000350181.3:n.1355-8G>A
ENST00000397163.7:c.1355-8G>A	ENSP00000380349.3:n.1355-8G>A
NM_000070.2:c.1355-8G>A	NP_000061.1:n.1355-8G>A
NM_024344.1:c.1355-8G>A	NP_077320.1:n.1355-8G>A
NM_173087.1:c.1211-8G>A	NP_775110.1:n.1211-8G>A
NM_000070.3:c.1355-8G>A MANE Select	NP_000061.1:n.1355-8G>A
NM_024344.2:c.1355-8G>A	NP_077320.1:n.1355-8G>A
NM_173087.2:c.1211-8G>A	NP_775110.1:n.1211-8G>A