Canonical Allele Identifier: CA413721590
Gene: PGK1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.77373648T>C (hg19) chrX:g.78118151T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78118151T>C , CM000685.2:g.78118151T>C GRCh38
NC_000023.10:g.77373648T>C , CM000685.1:g.77373648T>C GRCh37
NC_000023.9:g.77260304T>C NCBI36
NG_008862.1:g.18983T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000373316.5:c.622T>C MANE Select ENSP00000362413.4:p.Phe208Leu
ENST00000644362.1:c.538T>C ENSP00000496140.1:p.Phe180Leu
ENST00000373316.4:c.622T>C ENSP00000362413.4:p.Phe208Leu
ENST00000491291.1:n.614T>C
NM_000291.3:c.622T>C NP_000282.1:p.Phe208Leu
NM_000291.4:c.622T>C MANE Select NP_000282.1:p.Phe208Leu
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