Canonical Allele Identifier: CA1467014874
Gene: DCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71030579_71030580delinsAT , CM000666.2:g.71030579_71030580delinsAT GRCh38
NC_000004.11:g.71896296_71896297delinsAT , CM000666.1:g.71896296_71896297delinsAT GRCh37
NC_000004.10:g.72115160_72115161delinsAT NCBI36
NG_023303.1:g.42032_42033delinsAT

Transcript Alleles

HGVS Amino-acid change
ENST00000286648.10:c.*1201_*1202delinsAT MANE Select ENSP00000286648.5:n.*1201_*1202delinsAT
ENST00000286648.9:c.*1201_*1202delinsAT ENSP00000286648.5:n.*1201_*1202delinsAT
ENST00000503359.5:c.*1928_*1929delinsAT ENSP00000426389.1:n.*1928_*1929delinsAT
ENST00000504730.5:c.*1268_*1269delinsAT ENSP00000425578.1:n.*1268_*1269delinsAT
ENST00000504952.1:c.*1127_*1128delinsAT ENSP00000421508.1:n.*1127_*1128delinsAT
NM_000788.2:c.*1201_*1202delinsAT NP_000779.1:n.*1201_*1202delinsAT
NM_000788.3:c.*1201_*1202delinsAT MANE Select NP_000779.1:n.*1201_*1202delinsAT