Canonical Allele Identifier: CA413721200
Gene: PGK1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78117376A>T , CM000685.2:g.78117376A>T GRCh38
NC_000023.10:g.77372873A>T , CM000685.1:g.77372873A>T GRCh37
NC_000023.9:g.77259529A>T NCBI36
NG_008862.1:g.18208A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000373316.5:c.482A>T MANE Select ENSP00000362413.4:p.Tyr161Phe
ENST00000644362.1:c.398A>T ENSP00000496140.1:p.Tyr133Phe
ENST00000373316.4:c.482A>T ENSP00000362413.4:p.Tyr161Phe
ENST00000491291.1:n.474A>T
NM_000291.3:c.482A>T NP_000282.1:p.Tyr161Phe
NM_000291.4:c.482A>T MANE Select NP_000282.1:p.Tyr161Phe