Canonical Allele Identifier: CA1467014881
Gene: DCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71030612_71030616delinsAATTT , CM000666.2:g.71030612_71030616delinsAATTT GRCh38
NC_000004.11:g.71896329_71896333delinsAATTT , CM000666.1:g.71896329_71896333delinsAATTT GRCh37
NC_000004.10:g.72115193_72115197delinsAATTT NCBI36
NG_023303.1:g.42065_42069delinsAATTT

Transcript Alleles

HGVS Amino-acid change
ENST00000286648.10:c.*1234_*1238delinsAATTT MANE Select ENSP00000286648.5:n.*1234_*1238delinsAATT...
ENST00000286648.9:c.*1234_*1238delinsAATTT ENSP00000286648.5:n.*1234_*1238delinsAATT...
ENST00000503359.5:c.*1961_*1965delinsAATTT ENSP00000426389.1:n.*1961_*1965delinsAATT...
ENST00000504730.5:c.*1301_*1305delinsAATTT ENSP00000425578.1:n.*1301_*1305delinsAATT...
ENST00000504952.1:c.*1160_*1164delinsAATTT ENSP00000421508.1:n.*1160_*1164delinsAATT...
NM_000788.2:c.*1234_*1238delinsAATTT NP_000779.1:n.*1234_*1238delinsAATTT
NM_000788.3:c.*1234_*1238delinsAATTT MANE Select NP_000779.1:n.*1234_*1238delinsAATTT