Canonical Allele Identifier: CA1171578741
Gene: PGM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.63648541A= , CM000663.2:g.63648541A= GRCh38
NC_000001.10:g.64114212A= , CM000663.1:g.64114212A= GRCh37
NC_000001.9:g.63886800A= NCBI36
NG_016966.1:g.60266A=

Transcript Alleles

HGVS Amino-acid change
ENST00000371084.8:c.1169A= MANE Select ENSP00000360125.3:p.Asp390=
ENST00000650546.1:c.1169A= ENSP00000497812.1:p.Asp390=
ENST00000371083.4:c.1223A= ENSP00000360124.4:p.Asp408=
ENST00000371084.7:c.1169A= ENSP00000360125.3:p.Asp390=
ENST00000540265.5:c.578A= ENSP00000443449.1:p.Asp193=
NM_001172818.1:c.1223A= NP_001166289.1:p.Asp408=
NM_001172819.1:c.578A= NP_001166290.1:p.Asp193=
NM_002633.2:c.1169A= NP_002624.2:p.Asp390=
NM_002633.3:c.1169A= MANE Select NP_002624.2:p.Asp390=
NM_001172819.2:c.578A= NP_001166290.1:p.Asp193=