Canonical Allele Identifier: CA413719232
Gene: PGK1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.77369361G>C (hg19) chrX:g.78113864G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78113864G>C , CM000685.2:g.78113864G>C GRCh38
NC_000023.10:g.77369361G>C , CM000685.1:g.77369361G>C GRCh37
NC_000023.9:g.77256017G>C NCBI36
NG_008862.1:g.14696G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000373316.5:c.237G>C MANE Select ENSP00000362413.4:p.Glu79Asp
ENST00000644362.1:c.153G>C ENSP00000496140.1:p.Glu51Asp
ENST00000373316.4:c.237G>C ENSP00000362413.4:p.Glu79Asp
ENST00000491291.1:n.229G>C
NM_000291.3:c.237G>C NP_000282.1:p.Glu79Asp
NM_000291.4:c.237G>C MANE Select NP_000282.1:p.Glu79Asp
Search 100 bp 5'
Search 100 bp 3'