Canonical Allele Identifier: CA1144287796

Gene: PGM1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.63648637G= , CM000663.2:g.63648637G=	GRCh38
NC_000001.10:g.64114308G= , CM000663.1:g.64114308G=	GRCh37
NC_000001.9:g.63886896G=	NCBI36
NG_016966.1:g.60362G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000371084.8:c.1265G= MANE Select	ENSP00000360125.3:p.Arg422=
ENST00000650546.1:c.1265G=	ENSP00000497812.1:p.Arg422=
ENST00000371083.4:c.1319G=	ENSP00000360124.4:p.Arg440=
ENST00000371084.7:c.1265G=	ENSP00000360125.3:p.Arg422=
ENST00000540265.5:c.674G=	ENSP00000443449.1:p.Arg225=
NM_001172818.1:c.1319G=	NP_001166289.1:p.Arg440=
NM_001172819.1:c.674G=	NP_001166290.1:p.Arg225=
NM_002633.2:c.1265G=	NP_002624.2:p.Arg422=
NM_002633.3:c.1265G= MANE Select	NP_002624.2:p.Arg422=
NM_001172819.2:c.674G=	NP_001166290.1:p.Arg225=