Canonical Allele Identifier: CA1142355164
Gene: PGM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.63629431C= , CM000663.2:g.63629431C= GRCh38
NC_000001.10:g.64095102C= , CM000663.1:g.64095102C= GRCh37
NC_000001.9:g.63867690C= NCBI36
NG_016966.1:g.41156C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371084.8:c.253C= MANE Select ENSP00000360125.3:p.Arg85=
ENST00000650546.1:c.253C= ENSP00000497812.1:p.Arg85=
ENST00000371083.4:c.307C= ENSP00000360124.4:p.Arg103=
ENST00000371084.7:c.253C= ENSP00000360125.3:p.Arg85=
ENST00000540265.5:c.-339C= ENSP00000443449.1:n.-339C=
NM_001172818.1:c.307C= NP_001166289.1:p.Arg103=
NM_001172819.1:c.-339C= NP_001166290.1:n.-339C=
NM_002633.2:c.253C= NP_002624.2:p.Arg85=
NM_002633.3:c.253C= MANE Select NP_002624.2:p.Arg85=
NM_001172819.2:c.-339C= NP_001166290.1:n.-339C=