Canonical Allele Identifier: CA10459709
Gene: PGK1 HGNC NCBI

Linked Data

dbSNP Id: rs781868061
gnomAD v2: X-77372868-T-A
gnomAD v4: X-78117371-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78117371T>A , CM000685.2:g.78117371T>A GRCh38
NC_000023.10:g.77372868T>A , CM000685.1:g.77372868T>A GRCh37
NC_000023.9:g.77259524T>A NCBI36
NG_008862.1:g.18203T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000373316.5:c.477T>A MANE Select ENSP00000362413.4:p.Asp159Glu
ENST00000644362.1:c.393T>A ENSP00000496140.1:p.Asp131Glu
ENST00000373316.4:c.477T>A ENSP00000362413.4:p.Asp159Glu
ENST00000491291.1:n.469T>A
NM_000291.3:c.477T>A NP_000282.1:p.Asp159Glu
NM_000291.4:c.477T>A MANE Select NP_000282.1:p.Asp159Glu