Canonical Allele Identifier: CA2172714751

Gene: CAPN3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42402972G= , CM000677.2:g.42402972G=	GRCh38
NC_000015.9:g.42695170G= , CM000677.1:g.42695170G=	GRCh37
NC_000015.8:g.40482462G=	NCBI36
NG_008660.1:g.59870G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349748.8:c.1571G=	ENSP00000183936.4:p.Arg524=
ENST00000357568.8:c.1715G=	ENSP00000350181.3:p.Arg572=
ENST00000397163.8:c.1715G= MANE Select	ENSP00000380349.3:p.Arg572=
ENST00000466369.5:n.2224G=
ENST00000483208.5:n.2604G=
ENST00000495723.1:n.2604G=
ENST00000549793.5:n.1946G=
ENST00000638141.2:n.1586G=
ENST00000673646.1:c.179G=	ENSP00000501007.1:p.Arg60=
ENST00000673705.1:c.309+3320G=	ENSP00000501021.1:n.309+3320G=
ENST00000673813.1:n.580+57G=
ENST00000318023.11:c.1571G=	ENSP00000326281.8:p.Arg524=
ENST00000349748.7:c.1571G=	ENSP00000183936.4:p.Arg524=
ENST00000357568.7:c.1715G=	ENSP00000350181.3:p.Arg572=
ENST00000397163.7:c.1715G=	ENSP00000380349.3:p.Arg572=
ENST00000397200.8:c.179G=	ENSP00000380384.4:p.Arg60=
ENST00000567071.5:c.174G=
ENST00000569827.5:c.179G=	ENSP00000454379.1:p.Arg60=
NM_000070.2:c.1715G=	NP_000061.1:p.Arg572=
NM_024344.1:c.1715G=	NP_077320.1:p.Arg572=
NM_173087.1:c.1571G=	NP_775110.1:p.Arg524=
NM_173088.1:c.179G=	NP_775111.1:p.Arg60=
NM_000070.3:c.1715G= MANE Select	NP_000061.1:p.Arg572=
NM_024344.2:c.1715G=	NP_077320.1:p.Arg572=
NM_173087.2:c.1571G=	NP_775110.1:p.Arg524=
NM_173088.2:c.179G=	NP_775111.1:p.Arg60=