Canonical Allele Identifier: CA2172719039

Gene: CAPN3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42401728T= , CM000677.2:g.42401728T=	GRCh38
NC_000015.9:g.42693926T= , CM000677.1:g.42693926T=	GRCh37
NC_000015.8:g.40481218T=	NCBI36
NG_008660.1:g.58626T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349748.8:c.1298T=	ENSP00000183936.4:p.Leu433=
ENST00000357568.8:c.1442T=	ENSP00000350181.3:p.Leu481=
ENST00000397163.8:c.1442T= MANE Select	ENSP00000380349.3:p.Leu481=
ENST00000466369.5:n.1951T=
ENST00000483208.5:n.1673T=
ENST00000495723.1:n.1673T=
ENST00000549793.5:n.1673T=
ENST00000638141.2:n.1313T=
ENST00000673705.1:c.309+2076T=	ENSP00000501021.1:n.309+2076T=
ENST00000318023.11:c.1298T=	ENSP00000326281.8:p.Leu433=
ENST00000349748.7:c.1298T=	ENSP00000183936.4:p.Leu433=
ENST00000357568.7:c.1442T=	ENSP00000350181.3:p.Leu481=
ENST00000397163.7:c.1442T=	ENSP00000380349.3:p.Leu481=
NM_000070.2:c.1442T=	NP_000061.1:p.Leu481=
NM_024344.1:c.1442T=	NP_077320.1:p.Leu481=
NM_173087.1:c.1298T=	NP_775110.1:p.Leu433=
NM_000070.3:c.1442T= MANE Select	NP_000061.1:p.Leu481=
NM_024344.2:c.1442T=	NP_077320.1:p.Leu481=
NM_173087.2:c.1298T=	NP_775110.1:p.Leu433=