Canonical Allele Identifier: CA413721203
Gene: PGK1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.77372874T>A (hg19) chrX:g.78117377T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78117377T>A , CM000685.2:g.78117377T>A GRCh38
NC_000023.10:g.77372874T>A , CM000685.1:g.77372874T>A GRCh37
NC_000023.9:g.77259530T>A NCBI36
NG_008862.1:g.18209T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000373316.5:c.483T>A MANE Select ENSP00000362413.4:p.Tyr161Ter
ENST00000644362.1:c.399T>A ENSP00000496140.1:p.Tyr133Ter
ENST00000373316.4:c.483T>A ENSP00000362413.4:p.Tyr161Ter
ENST00000491291.1:n.475T>A
NM_000291.3:c.483T>A NP_000282.1:p.Tyr161Ter
NM_000291.4:c.483T>A MANE Select NP_000282.1:p.Tyr161Ter
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