Canonical Allele Identifier: CA2172714665

Gene: CAPN3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42402951A= , CM000677.2:g.42402951A=	GRCh38
NC_000015.9:g.42695149A= , CM000677.1:g.42695149A=	GRCh37
NC_000015.8:g.40482441A=	NCBI36
NG_008660.1:g.59849A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349748.8:c.1550A=	ENSP00000183936.4:p.Gln517=
ENST00000357568.8:c.1694A=	ENSP00000350181.3:p.Gln565=
ENST00000397163.8:c.1694A= MANE Select	ENSP00000380349.3:p.Gln565=
ENST00000466369.5:n.2203A=
ENST00000483208.5:n.2583A=
ENST00000495723.1:n.2583A=
ENST00000549793.5:n.1925A=
ENST00000638141.2:n.1565A=
ENST00000673646.1:c.158A=	ENSP00000501007.1:p.Gln53=
ENST00000673705.1:c.309+3299A=	ENSP00000501021.1:n.309+3299A=
ENST00000673813.1:n.580+36A=
ENST00000318023.11:c.1550A=	ENSP00000326281.8:p.Gln517=
ENST00000349748.7:c.1550A=	ENSP00000183936.4:p.Gln517=
ENST00000357568.7:c.1694A=	ENSP00000350181.3:p.Gln565=
ENST00000397163.7:c.1694A=	ENSP00000380349.3:p.Gln565=
ENST00000397200.8:c.158A=	ENSP00000380384.4:p.Gln53=
ENST00000567071.5:c.153A=
ENST00000569827.5:c.158A=	ENSP00000454379.1:p.Gln53=
NM_000070.2:c.1694A=	NP_000061.1:p.Gln565=
NM_024344.1:c.1694A=	NP_077320.1:p.Gln565=
NM_173087.1:c.1550A=	NP_775110.1:p.Gln517=
NM_173088.1:c.158A=	NP_775111.1:p.Gln53=
NM_000070.3:c.1694A= MANE Select	NP_000061.1:p.Gln565=
NM_024344.2:c.1694A=	NP_077320.1:p.Gln565=
NM_173087.2:c.1550A=	NP_775110.1:p.Gln517=
NM_173088.2:c.158A=	NP_775111.1:p.Gln53=