Canonical Allele Identifier: CA7511446

Gene: CAPN3

Linked Data

• ClinVar Variation Id: 1142203
• ClinVar RCV Id: RCV001479877
• dbSNP Id: rs745805303
• ExAC: 15:42695054 G / A
• gnomAD v2: 15-42695054-G-A
• gnomAD v3: 15-42402856-G-A
• gnomAD v4: 15-42402856-G-A
• MyVariant Identifiers: chr15:g.42695054G>A (hg19) ; chr15:g.42402856G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42402856G>A , CM000677.2:g.42402856G>A	GRCh38
NC_000015.9:g.42695054G>A , CM000677.1:g.42695054G>A	GRCh37
NC_000015.8:g.40482346G>A	NCBI36
NG_008660.1:g.59754G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349748.8:c.1455G>A	ENSP00000183936.4:p.Arg485=
ENST00000357568.8:c.1599G>A	ENSP00000350181.3:p.Arg533=
ENST00000397163.8:c.1599G>A MANE Select	ENSP00000380349.3:p.Arg533=
ENST00000466369.5:n.2108G>A
ENST00000483208.5:n.2488G>A
ENST00000495723.1:n.2488G>A
ENST00000549793.5:n.1830G>A
ENST00000638141.2:n.1470G>A
ENST00000673646.1:c.63G>A	ENSP00000501007.1:p.Arg21=
ENST00000673705.1:c.309+3204G>A	ENSP00000501021.1:n.309+3204G>A
ENST00000673813.1:n.521G>A
ENST00000318023.11:c.1455G>A	ENSP00000326281.8:p.Arg485=
ENST00000349748.7:c.1455G>A	ENSP00000183936.4:p.Arg485=
ENST00000357568.7:c.1599G>A	ENSP00000350181.3:p.Arg533=
ENST00000397163.7:c.1599G>A	ENSP00000380349.3:p.Arg533=
ENST00000397200.8:c.63G>A	ENSP00000380384.4:p.Arg21=
ENST00000567071.5:c.58G>A
ENST00000569827.5:c.63G>A	ENSP00000454379.1:p.Arg21=
NM_000070.2:c.1599G>A	NP_000061.1:p.Arg533=
NM_024344.1:c.1599G>A	NP_077320.1:p.Arg533=
NM_173087.1:c.1455G>A	NP_775110.1:p.Arg485=
NM_173088.1:c.63G>A	NP_775111.1:p.Arg21=
NM_000070.3:c.1599G>A MANE Select	NP_000061.1:p.Arg533=
NM_024344.2:c.1599G>A	NP_077320.1:p.Arg533=
NM_173087.2:c.1455G>A	NP_775110.1:p.Arg485=
NM_173088.2:c.63G>A	NP_775111.1:p.Arg21=