Canonical Allele Identifier: CA1171568748
Gene: PGM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.63623618A= , CM000663.2:g.63623618A= GRCh38
NC_000001.10:g.64089289A= , CM000663.1:g.64089289A= GRCh37
NC_000001.9:g.63861877A= NCBI36
NG_016966.1:g.35343A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371084.8:c.247-5807A= MANE Select ENSP00000360125.3:n.247-5807A=
ENST00000650546.1:c.247-5807A= ENSP00000497812.1:n.247-5807A=
ENST00000371083.4:c.158A= ENSP00000360124.4:p.Tyr53=
ENST00000371084.7:c.247-5807A= ENSP00000360125.3:n.247-5807A=
ENST00000540265.5:c.-345-5807A= ENSP00000443449.1:n.-345-5807A=
NM_001172818.1:c.158A= NP_001166289.1:p.Tyr53=
NM_001172819.1:c.-345-5807A= NP_001166290.1:n.-345-5807A=
NM_002633.2:c.247-5807A= NP_002624.2:n.247-5807A=
NM_002633.3:c.247-5807A= MANE Select NP_002624.2:n.247-5807A=
NM_001172819.2:c.-345-5807A= NP_001166290.1:n.-345-5807A=