Canonical Allele Identifier: CA2515798132
Gene: DCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71030644_71030645insAG , CM000666.2:g.71030644_71030645insAG GRCh38
NC_000004.11:g.71896361_71896362insAG , CM000666.1:g.71896361_71896362insAG GRCh37
NC_000004.10:g.72115225_72115226insAG NCBI36
NG_023303.1:g.42097_42098insAG

Transcript Alleles

HGVS Amino-acid change
ENST00000286648.10:c.*1266_*1267insAG MANE Select ENSP00000286648.5:n.*1266_*1267insAG
ENST00000286648.9:c.*1266_*1267insAG ENSP00000286648.5:n.*1266_*1267insAG
ENST00000503359.5:c.*1993_*1994insAG ENSP00000426389.1:n.*1993_*1994insAG
ENST00000504730.5:c.*1333_*1334insAG ENSP00000425578.1:n.*1333_*1334insAG
ENST00000504952.1:c.*1192_*1193insAG ENSP00000421508.1:n.*1192_*1193insAG
NM_000788.2:c.*1266_*1267insAG NP_000779.1:n.*1266_*1267insAG
NM_000788.3:c.*1266_*1267insAG MANE Select NP_000779.1:n.*1266_*1267insAG