Canonical Allele Identifier: CA2172697396

Gene: CAPN3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42359974A= , CM000677.2:g.42359974A=	GRCh38
NC_000015.9:g.42652172A= , CM000677.1:g.42652172A=	GRCh37
NC_000015.8:g.40439464A=	NCBI36
NG_008660.1:g.16872A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000349748.8:c.169A=	ENSP00000183936.4:p.Lys57=
ENST00000357568.8:c.169A=	ENSP00000350181.3:p.Lys57=
ENST00000397163.8:c.169A= MANE Select	ENSP00000380349.3:p.Lys57=
ENST00000466369.5:n.540+5521A=
ENST00000483208.5:n.540+5521A=
ENST00000495723.1:n.540+5521A=
ENST00000549793.5:n.540+5521A=
ENST00000318023.11:c.169A=	ENSP00000326281.8:p.Lys57=
ENST00000349748.7:c.169A=	ENSP00000183936.4:p.Lys57=
ENST00000357568.7:c.169A=	ENSP00000350181.3:p.Lys57=
ENST00000397163.7:c.169A=	ENSP00000380349.3:p.Lys57=
NM_000070.2:c.169A=	NP_000061.1:p.Lys57=
NM_024344.1:c.169A=	NP_077320.1:p.Lys57=
NM_173087.1:c.169A=	NP_775110.1:p.Lys57=
NM_000070.3:c.169A= MANE Select	NP_000061.1:p.Lys57=
NM_024344.2:c.169A=	NP_077320.1:p.Lys57=
NM_173087.2:c.169A=	NP_775110.1:p.Lys57=