Canonical Allele Identifier: CA1148440876
Gene: PGM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.63648531C= , CM000663.2:g.63648531C= GRCh38
NC_000001.10:g.64114202C= , CM000663.1:g.64114202C= GRCh37
NC_000001.9:g.63886790C= NCBI36
NG_016966.1:g.60256C=

Transcript Alleles

HGVS Amino-acid change
ENST00000371084.8:c.1159C= MANE Select ENSP00000360125.3:p.Arg387=
ENST00000650546.1:c.1159C= ENSP00000497812.1:p.Arg387=
ENST00000371083.4:c.1213C= ENSP00000360124.4:p.Arg405=
ENST00000371084.7:c.1159C= ENSP00000360125.3:p.Arg387=
ENST00000540265.5:c.568C= ENSP00000443449.1:p.Arg190=
NM_001172818.1:c.1213C= NP_001166289.1:p.Arg405=
NM_001172819.1:c.568C= NP_001166290.1:p.Arg190=
NM_002633.2:c.1159C= NP_002624.2:p.Arg387=
NM_002633.3:c.1159C= MANE Select NP_002624.2:p.Arg387=
NM_001172819.2:c.568C= NP_001166290.1:p.Arg190=