Canonical Allele Identifier: CA1467014781
Gene: DCK HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71030343T= , CM000666.2:g.71030343T= GRCh38
NC_000004.11:g.71896060T= , CM000666.1:g.71896060T= GRCh37
NC_000004.10:g.72114924T= NCBI36
NG_023303.1:g.41796T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000286648.10:c.*965T= MANE Select ENSP00000286648.5:n.*965T=
ENST00000286648.9:c.*965T= ENSP00000286648.5:n.*965T=
ENST00000503359.5:c.*1692T= ENSP00000426389.1:n.*1692T=
ENST00000504730.5:c.*1032T= ENSP00000425578.1:n.*1032T=
ENST00000504952.1:c.*891T= ENSP00000421508.1:n.*891T=
NM_000788.2:c.*965T= NP_000779.1:n.*965T=
NM_000788.3:c.*965T= MANE Select NP_000779.1:n.*965T=
Search 100 bp 5'
Search 100 bp 3'