Canonical Allele Identifier: CA1063948077
Gene: DCK HGNC NCBI

Linked Data

dbSNP Id: rs1740665505
gnomAD v3: 4-71030518-A-C
gnomAD v4: 4-71030518-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71030518A>C , CM000666.2:g.71030518A>C GRCh38
NC_000004.11:g.71896235A>C , CM000666.1:g.71896235A>C GRCh37
NC_000004.10:g.72115099A>C NCBI36
NG_023303.1:g.41971A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000286648.10:c.*1140A>C MANE Select ENSP00000286648.5:n.*1140A>C
ENST00000286648.9:c.*1140A>C ENSP00000286648.5:n.*1140A>C
ENST00000503359.5:c.*1867A>C ENSP00000426389.1:n.*1867A>C
ENST00000504730.5:c.*1207A>C ENSP00000425578.1:n.*1207A>C
ENST00000504952.1:c.*1066A>C ENSP00000421508.1:n.*1066A>C
NM_000788.2:c.*1140A>C NP_000779.1:n.*1140A>C
NM_000788.3:c.*1140A>C MANE Select NP_000779.1:n.*1140A>C
Search 100 bp 5'
Search 100 bp 3'