Canonical Allele Identifier: CA413716548
Gene: PGK1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.77378757G>T (hg19) chrX:g.78123260G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78123260G>T , CM000685.2:g.78123260G>T GRCh38
NC_000023.10:g.77378757G>T , CM000685.1:g.77378757G>T GRCh37
NC_000023.9:g.77265413G>T NCBI36
NG_008862.1:g.24092G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000373316.5:c.822G>T MANE Select ENSP00000362413.4:p.Glu274Asp
ENST00000644362.1:c.738G>T ENSP00000496140.1:p.Glu246Asp
ENST00000373316.4:c.822G>T ENSP00000362413.4:p.Glu274Asp
ENST00000474281.1:n.229G>T
NM_000291.3:c.822G>T NP_000282.1:p.Glu274Asp
NM_000291.4:c.822G>T MANE Select NP_000282.1:p.Glu274Asp
Search 100 bp 5'
Search 100 bp 3'