Canonical Allele Identifier: CA1144196978

Gene: PGM1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.63629443G= , CM000663.2:g.63629443G=	GRCh38
NC_000001.10:g.64095114G= , CM000663.1:g.64095114G=	GRCh37
NC_000001.9:g.63867702G=	NCBI36
NG_016966.1:g.41168G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371084.8:c.265G= MANE Select	ENSP00000360125.3:p.Gly89=
ENST00000650546.1:c.265G=	ENSP00000497812.1:p.Gly89=
ENST00000371083.4:c.319G=	ENSP00000360124.4:p.Gly107=
ENST00000371084.7:c.265G=	ENSP00000360125.3:p.Gly89=
ENST00000540265.5:c.-327G=	ENSP00000443449.1:n.-327G=
NM_001172818.1:c.319G=	NP_001166289.1:p.Gly107=
NM_001172819.1:c.-327G=	NP_001166290.1:n.-327G=
NM_002633.2:c.265G=	NP_002624.2:p.Gly89=
NM_002633.3:c.265G= MANE Select	NP_002624.2:p.Gly89=
NM_001172819.2:c.-327G=	NP_001166290.1:n.-327G=