Canonical Allele Identifier: CA413719124
Gene: PGK1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.77369341C>G (hg19) chrX:g.78113844C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78113844C>G , CM000685.2:g.78113844C>G GRCh38
NC_000023.10:g.77369341C>G , CM000685.1:g.77369341C>G GRCh37
NC_000023.9:g.77255997C>G NCBI36
NG_008862.1:g.14676C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000373316.5:c.217C>G MANE Select ENSP00000362413.4:p.Pro73Ala
ENST00000644362.1:c.133C>G ENSP00000496140.1:p.Pro45Ala
ENST00000373316.4:c.217C>G ENSP00000362413.4:p.Pro73Ala
ENST00000477335.5:n.353C>G
ENST00000491291.1:n.209C>G
NM_000291.3:c.217C>G NP_000282.1:p.Pro73Ala
NM_000291.4:c.217C>G MANE Select NP_000282.1:p.Pro73Ala
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