Canonical Allele Identifier: CA413718880
Gene: PGK1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.77369290A>C (hg19) chrX:g.78113793A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78113793A>C , CM000685.2:g.78113793A>C GRCh38
NC_000023.10:g.77369290A>C , CM000685.1:g.77369290A>C GRCh37
NC_000023.9:g.77255946A>C NCBI36
NG_008862.1:g.14625A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000373316.5:c.166A>C MANE Select ENSP00000362413.4:p.Lys56Gln
ENST00000644362.1:c.82A>C ENSP00000496140.1:p.Lys28Gln
ENST00000373316.4:c.166A>C ENSP00000362413.4:p.Lys56Gln
ENST00000477335.5:n.302A>C
ENST00000491291.1:n.158A>C
NM_000291.3:c.166A>C NP_000282.1:p.Lys56Gln
NM_000291.4:c.166A>C MANE Select NP_000282.1:p.Lys56Gln
Search 100 bp 5'
Search 100 bp 3'