Canonical Allele Identifier: CA16609217
Gene: PGK1 HGNC NCBI

Linked Data

ClinVar Variation Id: 391568
ClinVar RCV Id: RCV000417927
dbSNP Id: rs1057524140

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78113812G>A , CM000685.2:g.78113812G>A GRCh38
NC_000023.10:g.77369309G>A , CM000685.1:g.77369309G>A GRCh37
NC_000023.9:g.77255965G>A NCBI36
NG_008862.1:g.14644G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000373316.5:c.185G>A MANE Select ENSP00000362413.4:p.Ser62Asn
ENST00000644362.1:c.101G>A ENSP00000496140.1:p.Ser34Asn
ENST00000373316.4:c.185G>A ENSP00000362413.4:p.Ser62Asn
ENST00000477335.5:n.321G>A
ENST00000491291.1:n.177G>A
NM_000291.3:c.185G>A NP_000282.1:p.Ser62Asn
NM_000291.4:c.185G>A MANE Select NP_000282.1:p.Ser62Asn