Canonical Allele Identifier: CA413718904
Gene: PGK1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.77369294C>G (hg19) chrX:g.78113797C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78113797C>G , CM000685.2:g.78113797C>G GRCh38
NC_000023.10:g.77369294C>G , CM000685.1:g.77369294C>G GRCh37
NC_000023.9:g.77255950C>G NCBI36
NG_008862.1:g.14629C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000373316.5:c.170C>G MANE Select ENSP00000362413.4:p.Ser57Trp
ENST00000644362.1:c.86C>G ENSP00000496140.1:p.Ser29Trp
ENST00000373316.4:c.170C>G ENSP00000362413.4:p.Ser57Trp
ENST00000477335.5:n.306C>G
ENST00000491291.1:n.162C>G
NM_000291.3:c.170C>G NP_000282.1:p.Ser57Trp
NM_000291.4:c.170C>G MANE Select NP_000282.1:p.Ser57Trp
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