Canonical Allele Identifier: CA2581423360
Gene: DCK HGNC NCBI

Linked Data

gnomAD v4: 4-71030503-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71030503C>A , CM000666.2:g.71030503C>A GRCh38
NC_000004.11:g.71896220C>A , CM000666.1:g.71896220C>A GRCh37
NC_000004.10:g.72115084C>A NCBI36
NG_023303.1:g.41956C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000286648.10:c.*1125C>A MANE Select ENSP00000286648.5:n.*1125C>A
ENST00000286648.9:c.*1125C>A ENSP00000286648.5:n.*1125C>A
ENST00000503359.5:c.*1852C>A ENSP00000426389.1:n.*1852C>A
ENST00000504730.5:c.*1192C>A ENSP00000425578.1:n.*1192C>A
ENST00000504952.1:c.*1051C>A ENSP00000421508.1:n.*1051C>A
NM_000788.2:c.*1125C>A NP_000779.1:n.*1125C>A
NM_000788.3:c.*1125C>A MANE Select NP_000779.1:n.*1125C>A
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