Canonical Allele Identifier: CA413716734
Gene: PGK1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.77378795T>G (hg19) chrX:g.78123298T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78123298T>G , CM000685.2:g.78123298T>G GRCh38
NC_000023.10:g.77378795T>G , CM000685.1:g.77378795T>G GRCh37
NC_000023.9:g.77265451T>G NCBI36
NG_008862.1:g.24130T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000373316.5:c.860T>G MANE Select ENSP00000362413.4:p.Val287Gly
ENST00000644362.1:c.776T>G ENSP00000496140.1:p.Val259Gly
ENST00000373316.4:c.860T>G ENSP00000362413.4:p.Val287Gly
ENST00000474281.1:n.267T>G
NM_000291.3:c.860T>G NP_000282.1:p.Val287Gly
NM_000291.4:c.860T>G MANE Select NP_000282.1:p.Val287Gly
Search 100 bp 5'
Search 100 bp 3'