Canonical Allele Identifier: CA1467014939
Gene: DCK HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71030702G= , CM000666.2:g.71030702G= GRCh38
NC_000004.11:g.71896419G= , CM000666.1:g.71896419G= GRCh37
NC_000004.10:g.72115283G= NCBI36
NG_023303.1:g.42155G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000286648.10:c.*1324G= MANE Select ENSP00000286648.5:n.*1324G=
ENST00000286648.9:c.*1324G= ENSP00000286648.5:n.*1324G=
ENST00000503359.5:c.*2051G= ENSP00000426389.1:n.*2051G=
ENST00000504730.5:c.*1391G= ENSP00000425578.1:n.*1391G=
ENST00000504952.1:c.*1250G= ENSP00000421508.1:n.*1250G=
NM_000788.2:c.*1324G= NP_000779.1:n.*1324G=
NM_000788.3:c.*1324G= MANE Select NP_000779.1:n.*1324G=
Search 100 bp 5'
Search 100 bp 3'