Canonical Allele Identifier: CA1467014829
Gene: DCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71030461T= , CM000666.2:g.71030461T= GRCh38
NC_000004.11:g.71896178T= , CM000666.1:g.71896178T= GRCh37
NC_000004.10:g.72115042T= NCBI36
NG_023303.1:g.41914T=

Transcript Alleles

HGVS Amino-acid change
ENST00000286648.10:c.*1083T= MANE Select ENSP00000286648.5:n.*1083T=
ENST00000286648.9:c.*1083T= ENSP00000286648.5:n.*1083T=
ENST00000503359.5:c.*1810T= ENSP00000426389.1:n.*1810T=
ENST00000504730.5:c.*1150T= ENSP00000425578.1:n.*1150T=
ENST00000504952.1:c.*1009T= ENSP00000421508.1:n.*1009T=
NM_000788.2:c.*1083T= NP_000779.1:n.*1083T=
NM_000788.3:c.*1083T= MANE Select NP_000779.1:n.*1083T=