Canonical Allele Identifier: CA2172718988

Gene: CAPN3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42401669T= , CM000677.2:g.42401669T=	GRCh38
NC_000015.9:g.42693867T= , CM000677.1:g.42693867T=	GRCh37
NC_000015.8:g.40481159T=	NCBI36
NG_008660.1:g.58567T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000349748.8:c.1239T=	ENSP00000183936.4:p.Arg413=
ENST00000357568.8:c.1383T=	ENSP00000350181.3:p.Arg461=
ENST00000397163.8:c.1383T= MANE Select	ENSP00000380349.3:p.Arg461=
ENST00000466369.5:n.1892T=
ENST00000483208.5:n.1614T=
ENST00000495723.1:n.1614T=
ENST00000549793.5:n.1614T=
ENST00000638141.2:n.1254T=
ENST00000673705.1:c.309+2017T=	ENSP00000501021.1:n.309+2017T=
ENST00000318023.11:c.1239T=	ENSP00000326281.8:p.Arg413=
ENST00000349748.7:c.1239T=	ENSP00000183936.4:p.Arg413=
ENST00000357568.7:c.1383T=	ENSP00000350181.3:p.Arg461=
ENST00000397163.7:c.1383T=	ENSP00000380349.3:p.Arg461=
NM_000070.2:c.1383T=	NP_000061.1:p.Arg461=
NM_024344.1:c.1383T=	NP_077320.1:p.Arg461=
NM_173087.1:c.1239T=	NP_775110.1:p.Arg413=
NM_000070.3:c.1383T= MANE Select	NP_000061.1:p.Arg461=
NM_024344.2:c.1383T=	NP_077320.1:p.Arg461=
NM_173087.2:c.1239T=	NP_775110.1:p.Arg413=