Canonical Allele Identifier: CA1467014916
Gene: DCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71030668_71030670delinsACT , CM000666.2:g.71030668_71030670delinsACT GRCh38
NC_000004.11:g.71896385_71896387delinsACT , CM000666.1:g.71896385_71896387delinsACT GRCh37
NC_000004.10:g.72115249_72115251delinsACT NCBI36
NG_023303.1:g.42121_42123delinsACT

Transcript Alleles

HGVS Amino-acid Change
ENST00000286648.10:c.*1290_*1292delinsACT MANE Select ENSP00000286648.5:n.*1290_*1292delinsACT
ENST00000286648.9:c.*1290_*1292delinsACT ENSP00000286648.5:n.*1290_*1292delinsACT
ENST00000503359.5:c.*2017_*2019delinsACT ENSP00000426389.1:n.*2017_*2019delinsACT
ENST00000504730.5:c.*1357_*1359delinsACT ENSP00000425578.1:n.*1357_*1359delinsACT
ENST00000504952.1:c.*1216_*1218delinsACT ENSP00000421508.1:n.*1216_*1218delinsACT
NM_000788.2:c.*1290_*1292delinsACT NP_000779.1:n.*1290_*1292delinsACT
NM_000788.3:c.*1290_*1292delinsACT MANE Select NP_000779.1:n.*1290_*1292delinsACT