Canonical Allele Identifier: CA517379932
Gene: PGK1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.77373608G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78118111G>C , CM000685.2:g.78118111G>C GRCh38
NC_000023.10:g.77373608G>C , CM000685.1:g.77373608G>C GRCh37
NC_000023.9:g.77260264G>C NCBI36
NG_008862.1:g.18943G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000373316.5:c.582G>C MANE Select ENSP00000362413.4:p.Leu194=
ENST00000644362.1:c.498G>C ENSP00000496140.1:p.Leu166=
ENST00000373316.4:c.582G>C ENSP00000362413.4:p.Leu194=
ENST00000491291.1:n.574G>C
NM_000291.3:c.582G>C NP_000282.1:p.Leu194=
NM_000291.4:c.582G>C MANE Select NP_000282.1:p.Leu194=
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