Canonical Allele Identifier: CA2694155902
Gene: PGK1 HGNC NCBI

Linked Data

gnomAD v4: X-78118020-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78118020C>A , CM000685.2:g.78118020C>A GRCh38
NC_000023.10:g.77373517C>A , CM000685.1:g.77373517C>A GRCh37
NC_000023.9:g.77260173C>A NCBI36
NG_008862.1:g.18852C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000373316.5:c.522-31C>A MANE Select ENSP00000362413.4:n.522-31C>A
ENST00000644362.1:c.438-31C>A ENSP00000496140.1:n.438-31C>A
ENST00000373316.4:c.522-31C>A ENSP00000362413.4:n.522-31C>A
ENST00000491291.1:n.514-31C>A
NM_000291.3:c.522-31C>A NP_000282.1:n.522-31C>A
NM_000291.4:c.522-31C>A MANE Select NP_000282.1:n.522-31C>A
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