Canonical Allele Identifier: CA889781
Gene: PGM1 HGNC NCBI

Linked Data

dbSNP Id: rs527959572
gnomAD v2: 1-64114308-G-A
gnomAD v3: 1-63648637-G-A
gnomAD v4: 1-63648637-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.63648637G>A , CM000663.2:g.63648637G>A GRCh38
NC_000001.10:g.64114308G>A , CM000663.1:g.64114308G>A GRCh37
NC_000001.9:g.63886896G>A NCBI36
NG_016966.1:g.60362G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000371084.8:c.1265G>A MANE Select ENSP00000360125.3:p.Arg422Gln
ENST00000650546.1:c.1265G>A ENSP00000497812.1:p.Arg422Gln
ENST00000371083.4:c.1319G>A ENSP00000360124.4:p.Arg440Gln
ENST00000371084.7:c.1265G>A ENSP00000360125.3:p.Arg422Gln
ENST00000540265.5:c.674G>A ENSP00000443449.1:p.Arg225Gln
NM_001172818.1:c.1319G>A NP_001166289.1:p.Arg440Gln
NM_001172819.1:c.674G>A NP_001166290.1:p.Arg225Gln
NM_002633.2:c.1265G>A NP_002624.2:p.Arg422Gln
NM_002633.3:c.1265G>A MANE Select NP_002624.2:p.Arg422Gln
NM_001172819.2:c.674G>A NP_001166290.1:p.Arg225Gln