Canonical Allele Identifier: CA1467014935
Gene: DCK HGNC NCBI

Linked Data

dbSNP Id: rs1740671142

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71030694A>G , CM000666.2:g.71030694A>G GRCh38
NC_000004.11:g.71896411A>G , CM000666.1:g.71896411A>G GRCh37
NC_000004.10:g.72115275A>G NCBI36
NG_023303.1:g.42147A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000286648.10:c.*1316A>G MANE Select ENSP00000286648.5:n.*1316A>G
ENST00000286648.9:c.*1316A>G ENSP00000286648.5:n.*1316A>G
ENST00000503359.5:c.*2043A>G ENSP00000426389.1:n.*2043A>G
ENST00000504730.5:c.*1383A>G ENSP00000425578.1:n.*1383A>G
ENST00000504952.1:c.*1242A>G ENSP00000421508.1:n.*1242A>G
NM_000788.2:c.*1316A>G NP_000779.1:n.*1316A>G
NM_000788.3:c.*1316A>G MANE Select NP_000779.1:n.*1316A>G