Canonical Allele Identifier: CA1171568814

Gene: PGM1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.63623789T= , CM000663.2:g.63623789T=	GRCh38
NC_000001.10:g.64089460T= , CM000663.1:g.64089460T=	GRCh37
NC_000001.9:g.63862048T=	NCBI36
NG_016966.1:g.35514T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371084.8:c.247-5636T= MANE Select	ENSP00000360125.3:n.247-5636T=
ENST00000650546.1:c.247-5636T=	ENSP00000497812.1:n.247-5636T=
ENST00000371083.4:c.300+29T=	ENSP00000360124.4:n.300+29T=
ENST00000371084.7:c.247-5636T=	ENSP00000360125.3:n.247-5636T=
ENST00000540265.5:c.-345-5636T=	ENSP00000443449.1:n.-345-5636T=
NM_001172818.1:c.300+29T=	NP_001166289.1:n.300+29T=
NM_001172819.1:c.-345-5636T=	NP_001166290.1:n.-345-5636T=
NM_002633.2:c.247-5636T=	NP_002624.2:n.247-5636T=
NM_002633.3:c.247-5636T= MANE Select	NP_002624.2:n.247-5636T=
NM_001172819.2:c.-345-5636T=	NP_001166290.1:n.-345-5636T=