Canonical Allele Identifier: CA1171578742

Gene: PGM1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.63648542T= , CM000663.2:g.63648542T=	GRCh38
NC_000001.10:g.64114213T= , CM000663.1:g.64114213T=	GRCh37
NC_000001.9:g.63886801T=	NCBI36
NG_016966.1:g.60267T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000371084.8:c.1170T= MANE Select	ENSP00000360125.3:p.Asp390=
ENST00000650546.1:c.1170T=	ENSP00000497812.1:p.Asp390=
ENST00000371083.4:c.1224T=	ENSP00000360124.4:p.Asp408=
ENST00000371084.7:c.1170T=	ENSP00000360125.3:p.Asp390=
ENST00000540265.5:c.579T=	ENSP00000443449.1:p.Asp193=
NM_001172818.1:c.1224T=	NP_001166289.1:p.Asp408=
NM_001172819.1:c.579T=	NP_001166290.1:p.Asp193=
NM_002633.2:c.1170T=	NP_002624.2:p.Asp390=
NM_002633.3:c.1170T= MANE Select	NP_002624.2:p.Asp390=
NM_001172819.2:c.579T=	NP_001166290.1:p.Asp193=