Canonical Allele Identifier: CA2172714612

Gene: CAPN3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42402928G= , CM000677.2:g.42402928G=	GRCh38
NC_000015.9:g.42695126G= , CM000677.1:g.42695126G=	GRCh37
NC_000015.8:g.40482418G=	NCBI36
NG_008660.1:g.59826G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349748.8:c.1527G=	ENSP00000183936.4:p.Val509=
ENST00000357568.8:c.1671G=	ENSP00000350181.3:p.Val557=
ENST00000397163.8:c.1671G= MANE Select	ENSP00000380349.3:p.Val557=
ENST00000466369.5:n.2180G=
ENST00000483208.5:n.2560G=
ENST00000495723.1:n.2560G=
ENST00000549793.5:n.1902G=
ENST00000638141.2:n.1542G=
ENST00000673646.1:c.135G=	ENSP00000501007.1:p.Val45=
ENST00000673705.1:c.309+3276G=	ENSP00000501021.1:n.309+3276G=
ENST00000673813.1:n.580+13G=
ENST00000318023.11:c.1527G=	ENSP00000326281.8:p.Val509=
ENST00000349748.7:c.1527G=	ENSP00000183936.4:p.Val509=
ENST00000357568.7:c.1671G=	ENSP00000350181.3:p.Val557=
ENST00000397163.7:c.1671G=	ENSP00000380349.3:p.Val557=
ENST00000397200.8:c.135G=	ENSP00000380384.4:p.Val45=
ENST00000567071.5:c.130G=
ENST00000569827.5:c.135G=	ENSP00000454379.1:p.Val45=
NM_000070.2:c.1671G=	NP_000061.1:p.Val557=
NM_024344.1:c.1671G=	NP_077320.1:p.Val557=
NM_173087.1:c.1527G=	NP_775110.1:p.Val509=
NM_173088.1:c.135G=	NP_775111.1:p.Val45=
NM_000070.3:c.1671G= MANE Select	NP_000061.1:p.Val557=
NM_024344.2:c.1671G=	NP_077320.1:p.Val557=
NM_173087.2:c.1527G=	NP_775110.1:p.Val509=
NM_173088.2:c.135G=	NP_775111.1:p.Val45=