Canonical Allele Identifier: CA413720429
Gene: PGK1 HGNC NCBI

Linked Data

gnomAD v4: X-78117315-A-T
MyVariant Identifiers: chrX:g.77372812A>T (hg19) chrX:g.78117315A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78117315A>T , CM000685.2:g.78117315A>T GRCh38
NC_000023.10:g.77372812A>T , CM000685.1:g.77372812A>T GRCh37
NC_000023.9:g.77259468A>T NCBI36
NG_008862.1:g.18147A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000373316.5:c.421A>T MANE Select ENSP00000362413.4:p.Lys141Ter
ENST00000644362.1:c.337A>T ENSP00000496140.1:p.Lys113Ter
ENST00000373316.4:c.421A>T ENSP00000362413.4:p.Lys141Ter
ENST00000491291.1:n.413A>T
NM_000291.3:c.421A>T NP_000282.1:p.Lys141Ter
NM_000291.4:c.421A>T MANE Select NP_000282.1:p.Lys141Ter
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