Canonical Allele Identifier: CA2172710159

Gene: CAPN3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42388699T= , CM000677.2:g.42388699T=	GRCh38
NC_000015.9:g.42680897T= , CM000677.1:g.42680897T=	GRCh37
NC_000015.8:g.40468189T=	NCBI36
NG_008660.1:g.45597T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349748.8:c.633-229T=	ENSP00000183936.4:n.633-229T=
ENST00000357568.8:c.633-229T=	ENSP00000350181.3:n.633-229T=
ENST00000397163.8:c.633-229T= MANE Select	ENSP00000380349.3:n.633-229T=
ENST00000466369.5:n.1142-229T=
ENST00000483208.5:n.864-229T=
ENST00000495723.1:n.864-229T=
ENST00000549793.5:n.864-229T=
ENST00000638141.2:n.648-229T=
ENST00000673705.1:c.70+4147T=	ENSP00000501021.1:n.70+4147T=
ENST00000318023.11:c.633-229T=	ENSP00000326281.8:n.633-229T=
ENST00000349748.7:c.633-229T=	ENSP00000183936.4:n.633-229T=
ENST00000357568.7:c.633-229T=	ENSP00000350181.3:n.633-229T=
ENST00000397163.7:c.633-229T=	ENSP00000380349.3:n.633-229T=
NM_000070.2:c.633-229T=	NP_000061.1:n.633-229T=
NM_024344.1:c.633-229T=	NP_077320.1:n.633-229T=
NM_173087.1:c.633-229T=	NP_775110.1:n.633-229T=
NM_000070.3:c.633-229T= MANE Select	NP_000061.1:n.633-229T=
NM_024344.2:c.633-229T=	NP_077320.1:n.633-229T=
NM_173087.2:c.633-229T=	NP_775110.1:n.633-229T=