Canonical Allele Identifier: CA1467014860
Gene: DCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71030544_71030545delinsAT , CM000666.2:g.71030544_71030545delinsAT GRCh38
NC_000004.11:g.71896261_71896262delinsAT , CM000666.1:g.71896261_71896262delinsAT GRCh37
NC_000004.10:g.72115125_72115126delinsAT NCBI36
NG_023303.1:g.41997_41998delinsAT

Transcript Alleles

HGVS Amino-acid change
ENST00000286648.10:c.*1166_*1167delinsAT MANE Select ENSP00000286648.5:n.*1166_*1167delinsAT
ENST00000286648.9:c.*1166_*1167delinsAT ENSP00000286648.5:n.*1166_*1167delinsAT
ENST00000503359.5:c.*1893_*1894delinsAT ENSP00000426389.1:n.*1893_*1894delinsAT
ENST00000504730.5:c.*1233_*1234delinsAT ENSP00000425578.1:n.*1233_*1234delinsAT
ENST00000504952.1:c.*1092_*1093delinsAT ENSP00000421508.1:n.*1092_*1093delinsAT
NM_000788.2:c.*1166_*1167delinsAT NP_000779.1:n.*1166_*1167delinsAT
NM_000788.3:c.*1166_*1167delinsAT MANE Select NP_000779.1:n.*1166_*1167delinsAT