Canonical Allele Identifier: CA413716811
Gene: PGK1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.77378813A>G (hg19) chrX:g.78123316A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78123316A>G , CM000685.2:g.78123316A>G GRCh38
NC_000023.10:g.77378813A>G , CM000685.1:g.77378813A>G GRCh37
NC_000023.9:g.77265469A>G NCBI36
NG_008862.1:g.24148A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000373316.5:c.878A>G MANE Select ENSP00000362413.4:p.Asp293Gly
ENST00000644362.1:c.794A>G ENSP00000496140.1:p.Asp265Gly
ENST00000373316.4:c.878A>G ENSP00000362413.4:p.Asp293Gly
ENST00000474281.1:n.285A>G
NM_000291.3:c.878A>G NP_000282.1:p.Asp293Gly
NM_000291.4:c.878A>G MANE Select NP_000282.1:p.Asp293Gly
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