Canonical Allele Identifier: CA413718921
Gene: PGK1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.77369299G>A (hg19) chrX:g.78113802G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78113802G>A , CM000685.2:g.78113802G>A GRCh38
NC_000023.10:g.77369299G>A , CM000685.1:g.77369299G>A GRCh37
NC_000023.9:g.77255955G>A NCBI36
NG_008862.1:g.14634G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000373316.5:c.175G>A MANE Select ENSP00000362413.4:p.Val59Ile
ENST00000644362.1:c.91G>A ENSP00000496140.1:p.Val31Ile
ENST00000373316.4:c.175G>A ENSP00000362413.4:p.Val59Ile
ENST00000477335.5:n.311G>A
ENST00000491291.1:n.167G>A
NM_000291.3:c.175G>A NP_000282.1:p.Val59Ile
NM_000291.4:c.175G>A MANE Select NP_000282.1:p.Val59Ile
Search 100 bp 5'
Search 100 bp 3'