Canonical Allele Identifier: CA2706437907
Gene: DCK HGNC NCBI

Linked Data

dbSNP Id: rs2148921244
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71030465A>G , CM000666.2:g.71030465A>G GRCh38
NC_000004.11:g.71896182A>G , CM000666.1:g.71896182A>G GRCh37
NC_000004.10:g.72115046A>G NCBI36
NG_023303.1:g.41918A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000286648.10:c.*1087A>G MANE Select ENSP00000286648.5:n.*1087A>G
ENST00000286648.9:c.*1087A>G ENSP00000286648.5:n.*1087A>G
ENST00000503359.5:c.*1814A>G ENSP00000426389.1:n.*1814A>G
ENST00000504730.5:c.*1154A>G ENSP00000425578.1:n.*1154A>G
ENST00000504952.1:c.*1013A>G ENSP00000421508.1:n.*1013A>G
NM_000788.2:c.*1087A>G NP_000779.1:n.*1087A>G
NM_000788.3:c.*1087A>G MANE Select NP_000779.1:n.*1087A>G
Search 100 bp 5'
Search 100 bp 3'