Canonical Allele Identifier: CA2439138557
Gene: PGK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78117998T= , CM000685.2:g.78117998T= GRCh38
NC_000023.10:g.77373495T= , CM000685.1:g.77373495T= GRCh37
NC_000023.9:g.77260151T= NCBI36
NG_008862.1:g.18830T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000373316.5:c.522-53T= MANE Select ENSP00000362413.4:n.522-53T=
ENST00000644362.1:c.438-53T= ENSP00000496140.1:n.438-53T=
ENST00000373316.4:c.522-53T= ENSP00000362413.4:n.522-53T=
ENST00000491291.1:n.514-53T=
NM_000291.3:c.522-53T= NP_000282.1:n.522-53T=
NM_000291.4:c.522-53T= MANE Select NP_000282.1:n.522-53T=