Canonical Allele Identifier: CA1467014894
Gene: DCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71030629_71030632delinsTTTC , CM000666.2:g.71030629_71030632delinsTTTC GRCh38
NC_000004.11:g.71896346_71896349delinsTTTC , CM000666.1:g.71896346_71896349delinsTTTC GRCh37
NC_000004.10:g.72115210_72115213delinsTTTC NCBI36
NG_023303.1:g.42082_42085delinsTTTC

Transcript Alleles

HGVS Amino-acid change
ENST00000286648.10:c.*1251_*1254delinsTTTC MANE Select ENSP00000286648.5:n.*1251_*1254delinsTTTC...
ENST00000286648.9:c.*1251_*1254delinsTTTC ENSP00000286648.5:n.*1251_*1254delinsTTTC...
ENST00000503359.5:c.*1978_*1981delinsTTTC ENSP00000426389.1:n.*1978_*1981delinsTTTC...
ENST00000504730.5:c.*1318_*1321delinsTTTC ENSP00000425578.1:n.*1318_*1321delinsTTTC...
ENST00000504952.1:c.*1177_*1180delinsTTTC ENSP00000421508.1:n.*1177_*1180delinsTTTC...
NM_000788.2:c.*1251_*1254delinsTTTC NP_000779.1:n.*1251_*1254delinsTTTC
NM_000788.3:c.*1251_*1254delinsTTTC MANE Select NP_000779.1:n.*1251_*1254delinsTTTC