Canonical Allele Identifier: CA1148224360
Gene: PGM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.63634933G= , CM000663.2:g.63634933G= GRCh38
NC_000001.10:g.64100604G= , CM000663.1:g.64100604G= GRCh37
NC_000001.9:g.63873192G= NCBI36
NG_016966.1:g.46658G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371084.8:c.787G= MANE Select ENSP00000360125.3:p.Asp263=
ENST00000650546.1:c.787G= ENSP00000497812.1:p.Asp263=
ENST00000371083.4:c.841G= ENSP00000360124.4:p.Asp281=
ENST00000371084.7:c.787G= ENSP00000360125.3:p.Asp263=
ENST00000540265.5:c.196G= ENSP00000443449.1:p.Asp66=
NM_001172818.1:c.841G= NP_001166289.1:p.Asp281=
NM_001172819.1:c.196G= NP_001166290.1:p.Asp66=
NM_002633.2:c.787G= NP_002624.2:p.Asp263=
NM_002633.3:c.787G= MANE Select NP_002624.2:p.Asp263=
NM_001172819.2:c.196G= NP_001166290.1:p.Asp66=