Canonical Allele Identifier: CA1171579949

Gene: PGM1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.63651708A= , CM000663.2:g.63651708A=	GRCh38
NC_000001.10:g.64117379A= , CM000663.1:g.64117379A=	GRCh37
NC_000001.9:g.63889967A=	NCBI36
NG_016966.1:g.63433A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371084.8:c.1320A= MANE Select	ENSP00000360125.3:p.Lys440=
ENST00000650546.1:c.1320A=	ENSP00000497812.1:p.Lys440=
ENST00000371083.4:c.1374A=	ENSP00000360124.4:p.Lys458=
ENST00000371084.7:c.1320A=	ENSP00000360125.3:p.Lys440=
ENST00000483707.1:n.354A=
ENST00000540265.5:c.729A=	ENSP00000443449.1:p.Lys243=
NM_001172818.1:c.1374A=	NP_001166289.1:p.Lys458=
NM_001172819.1:c.729A=	NP_001166290.1:p.Lys243=
NM_002633.2:c.1320A=	NP_002624.2:p.Lys440=
NM_002633.3:c.1320A= MANE Select	NP_002624.2:p.Lys440=
NM_001172819.2:c.729A=	NP_001166290.1:p.Lys243=