Canonical Allele Identifier: CA413716922
Gene: PGK1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78123339G>T , CM000685.2:g.78123339G>T GRCh38
NC_000023.10:g.77378836G>T , CM000685.1:g.77378836G>T GRCh37
NC_000023.9:g.77265492G>T NCBI36
NG_008862.1:g.24171G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000373316.5:c.901G>T MANE Select ENSP00000362413.4:p.Ala301Ser
ENST00000644362.1:c.817G>T ENSP00000496140.1:p.Ala273Ser
ENST00000373316.4:c.901G>T ENSP00000362413.4:p.Ala301Ser
NM_000291.3:c.901G>T NP_000282.1:p.Ala301Ser
NM_000291.4:c.901G>T MANE Select NP_000282.1:p.Ala301Ser