Canonical Allele Identifier: CA1143403593
Gene: PGM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.63629432G= , CM000663.2:g.63629432G= GRCh38
NC_000001.10:g.64095103G= , CM000663.1:g.64095103G= GRCh37
NC_000001.9:g.63867691G= NCBI36
NG_016966.1:g.41157G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371084.8:c.254G= MANE Select ENSP00000360125.3:p.Arg85=
ENST00000650546.1:c.254G= ENSP00000497812.1:p.Arg85=
ENST00000371083.4:c.308G= ENSP00000360124.4:p.Arg103=
ENST00000371084.7:c.254G= ENSP00000360125.3:p.Arg85=
ENST00000540265.5:c.-338G= ENSP00000443449.1:n.-338G=
NM_001172818.1:c.308G= NP_001166289.1:p.Arg103=
NM_001172819.1:c.-338G= NP_001166290.1:n.-338G=
NM_002633.2:c.254G= NP_002624.2:p.Arg85=
NM_002633.3:c.254G= MANE Select NP_002624.2:p.Arg85=
NM_001172819.2:c.-338G= NP_001166290.1:n.-338G=