Canonical Allele Identifier: CA1467014826
Gene: DCK HGNC NCBI

Linked Data

dbSNP Id: rs1578433044
gnomAD v3: 4-71030444-C-A
gnomAD v4: 4-71030444-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71030444C>A , CM000666.2:g.71030444C>A GRCh38
NC_000004.11:g.71896161C>A , CM000666.1:g.71896161C>A GRCh37
NC_000004.10:g.72115025C>A NCBI36
NG_023303.1:g.41897C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000286648.10:c.*1066C>A MANE Select ENSP00000286648.5:n.*1066C>A
ENST00000286648.9:c.*1066C>A ENSP00000286648.5:n.*1066C>A
ENST00000503359.5:c.*1793C>A ENSP00000426389.1:n.*1793C>A
ENST00000504730.5:c.*1133C>A ENSP00000425578.1:n.*1133C>A
ENST00000504952.1:c.*992C>A ENSP00000421508.1:n.*992C>A
NM_000788.2:c.*1066C>A NP_000779.1:n.*1066C>A
NM_000788.3:c.*1066C>A MANE Select NP_000779.1:n.*1066C>A
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