Canonical Allele Identifier: CA413719056
Gene: PGK1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.77369328T>A (hg19) chrX:g.78113831T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78113831T>A , CM000685.2:g.78113831T>A GRCh38
NC_000023.10:g.77369328T>A , CM000685.1:g.77369328T>A GRCh37
NC_000023.9:g.77255984T>A NCBI36
NG_008862.1:g.14663T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000373316.5:c.204T>A MANE Select ENSP00000362413.4:p.Asp68Glu
ENST00000644362.1:c.120T>A ENSP00000496140.1:p.Asp40Glu
ENST00000373316.4:c.204T>A ENSP00000362413.4:p.Asp68Glu
ENST00000477335.5:n.340T>A
ENST00000491291.1:n.196T>A
NM_000291.3:c.204T>A NP_000282.1:p.Asp68Glu
NM_000291.4:c.204T>A MANE Select NP_000282.1:p.Asp68Glu
Search 100 bp 5'
Search 100 bp 3'