Canonical Allele Identifier: CA340649499
Community Standard Title: NM_002633.3(PGM1):c.689G>A (p.Gly230Glu)
Gene: PGM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.63634835G>A , CM000663.2:g.63634835G>A GRCh38
NC_000001.10:g.64100506G>A , CM000663.1:g.64100506G>A GRCh37
NC_000001.9:g.63873094G>A NCBI36
NG_016966.1:g.46560G>A

Transcript Alleles

HGVS Amino-acid Change
NM_002633.3:c.689G>A MANE Select NP_002624.2:p.Gly230Glu
ENST00000371084.8:c.689G>A MANE Select ENSP00000360125.3:p.Gly230Glu
NM_001172818.1:c.743G>A NP_001166289.1:p.Gly248Glu
NM_001172819.1:c.98G>A NP_001166290.1:p.Gly33Glu
NM_001172819.2:c.98G>A NP_001166290.1:p.Gly33Glu
NM_002633.2:c.689G>A NP_002624.2:p.Gly230Glu
ENST00000371083.4:c.743G>A ENSP00000360124.4:p.Gly248Glu
ENST00000371084.7:c.689G>A ENSP00000360125.3:p.Gly230Glu
ENST00000540265.5:c.98G>A ENSP00000443449.1:p.Gly33Glu
ENST00000650546.1:c.689G>A ENSP00000497812.1:p.Gly230Glu