Canonical Allele Identifier: CA1171571113

Gene: PGM1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.63629526C= , CM000663.2:g.63629526C=	GRCh38
NC_000001.10:g.64095197C= , CM000663.1:g.64095197C=	GRCh37
NC_000001.9:g.63867785C=	NCBI36
NG_016966.1:g.41251C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000371084.8:c.348C= MANE Select	ENSP00000360125.3:p.Ala116=
ENST00000650546.1:c.348C=	ENSP00000497812.1:p.Ala116=
ENST00000371083.4:c.402C=	ENSP00000360124.4:p.Ala134=
ENST00000371084.7:c.348C=	ENSP00000360125.3:p.Ala116=
ENST00000540265.5:c.-244C=	ENSP00000443449.1:n.-244C=
NM_001172818.1:c.402C=	NP_001166289.1:p.Ala134=
NM_001172819.1:c.-244C=	NP_001166290.1:n.-244C=
NM_002633.2:c.348C=	NP_002624.2:p.Ala116=
NM_002633.3:c.348C= MANE Select	NP_002624.2:p.Ala116=
NM_001172819.2:c.-244C=	NP_001166290.1:n.-244C=