Canonical Allele Identifier: CA1467014924
Gene: DCK HGNC NCBI

Linked Data

dbSNP Id: rs1740670671
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71030673T>C , CM000666.2:g.71030673T>C GRCh38
NC_000004.11:g.71896390T>C , CM000666.1:g.71896390T>C GRCh37
NC_000004.10:g.72115254T>C NCBI36
NG_023303.1:g.42126T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000286648.10:c.*1295T>C MANE Select ENSP00000286648.5:n.*1295T>C
ENST00000286648.9:c.*1295T>C ENSP00000286648.5:n.*1295T>C
ENST00000503359.5:c.*2022T>C ENSP00000426389.1:n.*2022T>C
ENST00000504730.5:c.*1362T>C ENSP00000425578.1:n.*1362T>C
ENST00000504952.1:c.*1221T>C ENSP00000421508.1:n.*1221T>C
NM_000788.2:c.*1295T>C NP_000779.1:n.*1295T>C
NM_000788.3:c.*1295T>C MANE Select NP_000779.1:n.*1295T>C
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