Canonical Allele Identifier: CA1467014902
Gene: DCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71030640_71030641delinsTA , CM000666.2:g.71030640_71030641delinsTA GRCh38
NC_000004.11:g.71896357_71896358delinsTA , CM000666.1:g.71896357_71896358delinsTA GRCh37
NC_000004.10:g.72115221_72115222delinsTA NCBI36
NG_023303.1:g.42093_42094delinsTA

Transcript Alleles

HGVS Amino-acid change
ENST00000286648.10:c.*1262_*1263delinsTA MANE Select ENSP00000286648.5:n.*1262_*1263delinsTA
ENST00000286648.9:c.*1262_*1263delinsTA ENSP00000286648.5:n.*1262_*1263delinsTA
ENST00000503359.5:c.*1989_*1990delinsTA ENSP00000426389.1:n.*1989_*1990delinsTA
ENST00000504730.5:c.*1329_*1330delinsTA ENSP00000425578.1:n.*1329_*1330delinsTA
ENST00000504952.1:c.*1188_*1189delinsTA ENSP00000421508.1:n.*1188_*1189delinsTA
NM_000788.2:c.*1262_*1263delinsTA NP_000779.1:n.*1262_*1263delinsTA
NM_000788.3:c.*1262_*1263delinsTA MANE Select NP_000779.1:n.*1262_*1263delinsTA