Canonical Allele Identifier: CA413721389
Gene: PGK1 HGNC NCBI

Linked Data

gnomAD v4: X-78118069-T-A
MyVariant Identifiers: chrX:g.77373566T>A (hg19) chrX:g.78118069T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78118069T>A , CM000685.2:g.78118069T>A GRCh38
NC_000023.10:g.77373566T>A , CM000685.1:g.77373566T>A GRCh37
NC_000023.9:g.77260222T>A NCBI36
NG_008862.1:g.18901T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000373316.5:c.540T>A MANE Select ENSP00000362413.4:p.Asn180Lys
ENST00000644362.1:c.456T>A ENSP00000496140.1:p.Asn152Lys
ENST00000373316.4:c.540T>A ENSP00000362413.4:p.Asn180Lys
ENST00000491291.1:n.532T>A
NM_000291.3:c.540T>A NP_000282.1:p.Asn180Lys
NM_000291.4:c.540T>A MANE Select NP_000282.1:p.Asn180Lys
Search 100 bp 5'
Search 100 bp 3'