Canonical Allele Identifier: CA2172712734

Gene: CAPN3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42394140C= , CM000677.2:g.42394140C=	GRCh38
NC_000015.9:g.42686338C= , CM000677.1:g.42686338C=	GRCh37
NC_000015.8:g.40473630C=	NCBI36
NG_008660.1:g.51038C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349748.8:c.886-116C=	ENSP00000183936.4:n.886-116C=
ENST00000357568.8:c.1030-116C=	ENSP00000350181.3:n.1030-116C=
ENST00000397163.8:c.1030-116C= MANE Select	ENSP00000380349.3:n.1030-116C=
ENST00000466369.5:n.1539-116C=
ENST00000483208.5:n.1261-116C=
ENST00000495723.1:n.1261-116C=
ENST00000549793.5:n.1261-116C=
ENST00000638141.2:n.901-116C=
ENST00000673658.1:n.14-116C=
ENST00000673705.1:c.71-2660C=	ENSP00000501021.1:n.71-2660C=
ENST00000318023.11:c.886-116C=	ENSP00000326281.8:n.886-116C=
ENST00000349748.7:c.886-116C=	ENSP00000183936.4:n.886-116C=
ENST00000357568.7:c.1030-116C=	ENSP00000350181.3:n.1030-116C=
ENST00000397163.7:c.1030-116C=	ENSP00000380349.3:n.1030-116C=
NM_000070.2:c.1030-116C=	NP_000061.1:n.1030-116C=
NM_024344.1:c.1030-116C=	NP_077320.1:n.1030-116C=
NM_173087.1:c.886-116C=	NP_775110.1:n.886-116C=
NM_000070.3:c.1030-116C= MANE Select	NP_000061.1:n.1030-116C=
NM_024344.2:c.1030-116C=	NP_077320.1:n.1030-116C=
NM_173087.2:c.886-116C=	NP_775110.1:n.886-116C=