Canonical Allele Identifier: CA1467014933
Gene: DCK HGNC NCBI

Linked Data

dbSNP Id: rs1740671207

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71030698dup , CM000666.2:g.71030698dup GRCh38
NC_000004.11:g.71896415dup , CM000666.1:g.71896415dup GRCh37
NC_000004.10:g.72115279dup NCBI36
NG_023303.1:g.42151dup

Transcript Alleles

HGVS Amino-acid change
ENST00000286648.10:c.*1320dup MANE Select ENSP00000286648.5:n.*1320dup
ENST00000286648.9:c.*1320dup ENSP00000286648.5:n.*1320dup
ENST00000503359.5:c.*2047dup ENSP00000426389.1:n.*2047dup
ENST00000504730.5:c.*1387dup ENSP00000425578.1:n.*1387dup
ENST00000504952.1:c.*1246dup ENSP00000421508.1:n.*1246dup
NM_000788.2:c.*1320dup NP_000779.1:n.*1320dup
NM_000788.3:c.*1320dup MANE Select NP_000779.1:n.*1320dup