Canonical Allele Identifier: CA1148716697
Gene: PGM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.63648636C= , CM000663.2:g.63648636C= GRCh38
NC_000001.10:g.64114307C= , CM000663.1:g.64114307C= GRCh37
NC_000001.9:g.63886895C= NCBI36
NG_016966.1:g.60361C=

Transcript Alleles

HGVS Amino-acid change
ENST00000371084.8:c.1264C= MANE Select ENSP00000360125.3:p.Arg422=
ENST00000650546.1:c.1264C= ENSP00000497812.1:p.Arg422=
ENST00000371083.4:c.1318C= ENSP00000360124.4:p.Arg440=
ENST00000371084.7:c.1264C= ENSP00000360125.3:p.Arg422=
ENST00000540265.5:c.673C= ENSP00000443449.1:p.Arg225=
NM_001172818.1:c.1318C= NP_001166289.1:p.Arg440=
NM_001172819.1:c.673C= NP_001166290.1:p.Arg225=
NM_002633.2:c.1264C= NP_002624.2:p.Arg422=
NM_002633.3:c.1264C= MANE Select NP_002624.2:p.Arg422=
NM_001172819.2:c.673C= NP_001166290.1:p.Arg225=