Canonical Allele Identifier: CA517379930
Gene: PGK1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.77373606C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78118109C>T , CM000685.2:g.78118109C>T GRCh38
NC_000023.10:g.77373606C>T , CM000685.1:g.77373606C>T GRCh37
NC_000023.9:g.77260262C>T NCBI36
NG_008862.1:g.18941C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000373316.5:c.580C>T MANE Select ENSP00000362413.4:p.Leu194=
ENST00000644362.1:c.496C>T ENSP00000496140.1:p.Leu166=
ENST00000373316.4:c.580C>T ENSP00000362413.4:p.Leu194=
ENST00000491291.1:n.572C>T
NM_000291.3:c.580C>T NP_000282.1:p.Leu194=
NM_000291.4:c.580C>T MANE Select NP_000282.1:p.Leu194=