Canonical Allele Identifier: CA1467014828
Gene: DCK HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71030458G= , CM000666.2:g.71030458G= GRCh38
NC_000004.11:g.71896175G= , CM000666.1:g.71896175G= GRCh37
NC_000004.10:g.72115039G= NCBI36
NG_023303.1:g.41911G=

Transcript Alleles

HGVS Amino-acid change
ENST00000286648.10:c.*1080G= MANE Select ENSP00000286648.5:n.*1080G=
ENST00000286648.9:c.*1080G= ENSP00000286648.5:n.*1080G=
ENST00000503359.5:c.*1807G= ENSP00000426389.1:n.*1807G=
ENST00000504730.5:c.*1147G= ENSP00000425578.1:n.*1147G=
ENST00000504952.1:c.*1006G= ENSP00000421508.1:n.*1006G=
NM_000788.2:c.*1080G= NP_000779.1:n.*1080G=
NM_000788.3:c.*1080G= MANE Select NP_000779.1:n.*1080G=
Search 100 bp 5'
Search 100 bp 3'