Canonical Allele Identifier: CA517473269
Gene: PGK1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.77369298A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78113801A>T , CM000685.2:g.78113801A>T GRCh38
NC_000023.10:g.77369298A>T , CM000685.1:g.77369298A>T GRCh37
NC_000023.9:g.77255954A>T NCBI36
NG_008862.1:g.14633A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000373316.5:c.174A>T MANE Select ENSP00000362413.4:p.Val58=
ENST00000644362.1:c.90A>T ENSP00000496140.1:p.Val30=
ENST00000373316.4:c.174A>T ENSP00000362413.4:p.Val58=
ENST00000477335.5:n.310A>T
ENST00000491291.1:n.166A>T
NM_000291.3:c.174A>T NP_000282.1:p.Val58=
NM_000291.4:c.174A>T MANE Select NP_000282.1:p.Val58=