Canonical Allele Identifier: CA517380833
Gene: PGK1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.77378829T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78123332T>C , CM000685.2:g.78123332T>C GRCh38
NC_000023.10:g.77378829T>C , CM000685.1:g.77378829T>C GRCh37
NC_000023.9:g.77265485T>C NCBI36
NG_008862.1:g.24164T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000373316.5:c.894T>C MANE Select ENSP00000362413.4:p.Thr298=
ENST00000644362.1:c.810T>C ENSP00000496140.1:p.Thr270=
ENST00000373316.4:c.894T>C ENSP00000362413.4:p.Thr298=
ENST00000474281.1:n.301T>C
NM_000291.3:c.894T>C NP_000282.1:p.Thr298=
NM_000291.4:c.894T>C MANE Select NP_000282.1:p.Thr298=
Search 100 bp 5'
Search 100 bp 3'