Canonical Allele Identifier: CA413719114
Gene: PGK1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.77369340G>A (hg19) chrX:g.78113843G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78113843G>A , CM000685.2:g.78113843G>A GRCh38
NC_000023.10:g.77369340G>A , CM000685.1:g.77369340G>A GRCh37
NC_000023.9:g.77255996G>A NCBI36
NG_008862.1:g.14675G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000373316.5:c.216G>A MANE Select ENSP00000362413.4:p.Met72Ile
ENST00000644362.1:c.132G>A ENSP00000496140.1:p.Met44Ile
ENST00000373316.4:c.216G>A ENSP00000362413.4:p.Met72Ile
ENST00000477335.5:n.352G>A
ENST00000491291.1:n.208G>A
NM_000291.3:c.216G>A NP_000282.1:p.Met72Ile
NM_000291.4:c.216G>A MANE Select NP_000282.1:p.Met72Ile
Search 100 bp 5'
Search 100 bp 3'