Canonical Allele Identifier: CA517379652
Gene: PGK1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.77372811T>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78117314T>A , CM000685.2:g.78117314T>A GRCh38
NC_000023.10:g.77372811T>A , CM000685.1:g.77372811T>A GRCh37
NC_000023.9:g.77259467T>A NCBI36
NG_008862.1:g.18146T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000373316.5:c.420T>A MANE Select ENSP00000362413.4:p.Val140=
ENST00000644362.1:c.336T>A ENSP00000496140.1:p.Val112=
ENST00000373316.4:c.420T>A ENSP00000362413.4:p.Val140=
ENST00000491291.1:n.412T>A
NM_000291.3:c.420T>A NP_000282.1:p.Val140=
NM_000291.4:c.420T>A MANE Select NP_000282.1:p.Val140=
Search 100 bp 5'
Search 100 bp 3'