Canonical Allele Identifier: CA1148448848

Gene: PGM1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.63648469A= , CM000663.2:g.63648469A=	GRCh38
NC_000001.10:g.64114140A= , CM000663.1:g.64114140A=	GRCh37
NC_000001.9:g.63886728A=	NCBI36
NG_016966.1:g.60194A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371084.8:c.1145-48A= MANE Select	ENSP00000360125.3:n.1145-48A=
ENST00000650546.1:c.1145-48A=	ENSP00000497812.1:n.1145-48A=
ENST00000371083.4:c.1199-48A=	ENSP00000360124.4:n.1199-48A=
ENST00000371084.7:c.1145-48A=	ENSP00000360125.3:n.1145-48A=
ENST00000540265.5:c.554-48A=	ENSP00000443449.1:n.554-48A=
NM_001172818.1:c.1199-48A=	NP_001166289.1:n.1199-48A=
NM_001172819.1:c.554-48A=	NP_001166290.1:n.554-48A=
NM_002633.2:c.1145-48A=	NP_002624.2:n.1145-48A=
NM_002633.3:c.1145-48A= MANE Select	NP_002624.2:n.1145-48A=
NM_001172819.2:c.554-48A=	NP_001166290.1:n.554-48A=