Canonical Allele Identifier: CA1141580822

Gene: PGM1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.63629521A= , CM000663.2:g.63629521A=	GRCh38
NC_000001.10:g.64095192A= , CM000663.1:g.64095192A=	GRCh37
NC_000001.9:g.63867780A=	NCBI36
NG_016966.1:g.41246A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000371084.8:c.343A= MANE Select	ENSP00000360125.3:p.Thr115=
ENST00000650546.1:c.343A=	ENSP00000497812.1:p.Thr115=
ENST00000371083.4:c.397A=	ENSP00000360124.4:p.Thr133=
ENST00000371084.7:c.343A=	ENSP00000360125.3:p.Thr115=
ENST00000540265.5:c.-249A=	ENSP00000443449.1:n.-249A=
NM_001172818.1:c.397A=	NP_001166289.1:p.Thr133=
NM_001172819.1:c.-249A=	NP_001166290.1:n.-249A=
NM_002633.2:c.343A=	NP_002624.2:p.Thr115=
NM_002633.3:c.343A= MANE Select	NP_002624.2:p.Thr115=
NM_001172819.2:c.-249A=	NP_001166290.1:n.-249A=