Canonical Allele Identifier: CA2694155886
Gene: PGK1 HGNC NCBI

Linked Data

gnomAD v4: X-78118004-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78118004G>A , CM000685.2:g.78118004G>A GRCh38
NC_000023.10:g.77373501G>A , CM000685.1:g.77373501G>A GRCh37
NC_000023.9:g.77260157G>A NCBI36
NG_008862.1:g.18836G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000373316.5:c.522-47G>A MANE Select ENSP00000362413.4:n.522-47G>A
ENST00000644362.1:c.438-47G>A ENSP00000496140.1:n.438-47G>A
ENST00000373316.4:c.522-47G>A ENSP00000362413.4:n.522-47G>A
ENST00000491291.1:n.514-47G>A
NM_000291.3:c.522-47G>A NP_000282.1:n.522-47G>A
NM_000291.4:c.522-47G>A MANE Select NP_000282.1:n.522-47G>A