Canonical Allele Identifier: CA1171571126
Gene: PGM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.63629548A= , CM000663.2:g.63629548A= GRCh38
NC_000001.10:g.64095219A= , CM000663.1:g.64095219A= GRCh37
NC_000001.9:g.63867807A= NCBI36
NG_016966.1:g.41273A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371084.8:c.370A= MANE Select ENSP00000360125.3:p.Asn124=
ENST00000650546.1:c.370A= ENSP00000497812.1:p.Asn124=
ENST00000371083.4:c.424A= ENSP00000360124.4:p.Asn142=
ENST00000371084.7:c.370A= ENSP00000360125.3:p.Asn124=
ENST00000540265.5:c.-222A= ENSP00000443449.1:n.-222A=
NM_001172818.1:c.424A= NP_001166289.1:p.Asn142=
NM_001172819.1:c.-222A= NP_001166290.1:n.-222A=
NM_002633.2:c.370A= NP_002624.2:p.Asn124=
NM_002633.3:c.370A= MANE Select NP_002624.2:p.Asn124=
NM_001172819.2:c.-222A= NP_001166290.1:n.-222A=