Canonical Allele Identifier: CA1467014839
Gene: DCK HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71030489T= , CM000666.2:g.71030489T= GRCh38
NC_000004.11:g.71896206T= , CM000666.1:g.71896206T= GRCh37
NC_000004.10:g.72115070T= NCBI36
NG_023303.1:g.41942T=

Transcript Alleles

HGVS Amino-acid change
ENST00000286648.10:c.*1111T= MANE Select ENSP00000286648.5:n.*1111T=
ENST00000286648.9:c.*1111T= ENSP00000286648.5:n.*1111T=
ENST00000503359.5:c.*1838T= ENSP00000426389.1:n.*1838T=
ENST00000504730.5:c.*1178T= ENSP00000425578.1:n.*1178T=
ENST00000504952.1:c.*1037T= ENSP00000421508.1:n.*1037T=
NM_000788.2:c.*1111T= NP_000779.1:n.*1111T=
NM_000788.3:c.*1111T= MANE Select NP_000779.1:n.*1111T=
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