Canonical Allele Identifier: CA1139835933
Gene: PGM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.63629440A= , CM000663.2:g.63629440A= GRCh38
NC_000001.10:g.64095111A= , CM000663.1:g.64095111A= GRCh37
NC_000001.9:g.63867699A= NCBI36
NG_016966.1:g.41165A=

Transcript Alleles

HGVS Amino-acid change
ENST00000371084.8:c.262A= MANE Select ENSP00000360125.3:p.Ile88=
ENST00000650546.1:c.262A= ENSP00000497812.1:p.Ile88=
ENST00000371083.4:c.316A= ENSP00000360124.4:p.Ile106=
ENST00000371084.7:c.262A= ENSP00000360125.3:p.Ile88=
ENST00000540265.5:c.-330A= ENSP00000443449.1:n.-330A=
NM_001172818.1:c.316A= NP_001166289.1:p.Ile106=
NM_001172819.1:c.-330A= NP_001166290.1:n.-330A=
NM_002633.2:c.262A= NP_002624.2:p.Ile88=
NM_002633.3:c.262A= MANE Select NP_002624.2:p.Ile88=
NM_001172819.2:c.-330A= NP_001166290.1:n.-330A=