Canonical Allele Identifier: CA1467014866
Gene: DCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71030559_71030561delinsCTG , CM000666.2:g.71030559_71030561delinsCTG GRCh38
NC_000004.11:g.71896276_71896278delinsCTG , CM000666.1:g.71896276_71896278delinsCTG GRCh37
NC_000004.10:g.72115140_72115142delinsCTG NCBI36
NG_023303.1:g.42012_42014delinsCTG

Transcript Alleles

HGVS Amino-acid change
ENST00000286648.10:c.*1181_*1183delinsCTG MANE Select ENSP00000286648.5:n.*1181_*1183delinsCTG
ENST00000286648.9:c.*1181_*1183delinsCTG ENSP00000286648.5:n.*1181_*1183delinsCTG
ENST00000503359.5:c.*1908_*1910delinsCTG ENSP00000426389.1:n.*1908_*1910delinsCTG
ENST00000504730.5:c.*1248_*1250delinsCTG ENSP00000425578.1:n.*1248_*1250delinsCTG
ENST00000504952.1:c.*1107_*1109delinsCTG ENSP00000421508.1:n.*1107_*1109delinsCTG
NM_000788.2:c.*1181_*1183delinsCTG NP_000779.1:n.*1181_*1183delinsCTG
NM_000788.3:c.*1181_*1183delinsCTG MANE Select NP_000779.1:n.*1181_*1183delinsCTG