Canonical Allele Identifier: CA2563831019
Gene: DCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71030642_71030643insTGAG , CM000666.2:g.71030642_71030643insTGAG GRCh38
NC_000004.11:g.71896359_71896360insTGAG , CM000666.1:g.71896359_71896360insTGAG GRCh37
NC_000004.10:g.72115223_72115224insTGAG NCBI36
NG_023303.1:g.42095_42096insTGAG

Transcript Alleles

HGVS Amino-acid change
ENST00000286648.10:c.*1264_*1265insTGAG MANE Select ENSP00000286648.5:n.*1264_*1265insTGAG
ENST00000286648.9:c.*1264_*1265insTGAG ENSP00000286648.5:n.*1264_*1265insTGAG
ENST00000503359.5:c.*1991_*1992insTGAG ENSP00000426389.1:n.*1991_*1992insTGAG
ENST00000504730.5:c.*1331_*1332insTGAG ENSP00000425578.1:n.*1331_*1332insTGAG
ENST00000504952.1:c.*1190_*1191insTGAG ENSP00000421508.1:n.*1190_*1191insTGAG
NM_000788.2:c.*1264_*1265insTGAG NP_000779.1:n.*1264_*1265insTGAG
NM_000788.3:c.*1264_*1265insTGAG MANE Select NP_000779.1:n.*1264_*1265insTGAG