Canonical Allele Identifier: CA99415215
Gene: DCK HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1803484

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71030626A>G , CM000666.2:g.71030626A>G GRCh38
NC_000004.11:g.71896343A>G , CM000666.1:g.71896343A>G GRCh37
NC_000004.10:g.72115207A>G NCBI36
NG_023303.1:g.42079A>G

Transcript Alleles

HGVS Amino-acid change
NM_000788.2:c.*1248A>G VV NP_000779.1:p.=
NM_000788.3:c.*1248A>G VV MANE Preferred
ENST00000286648.9:c.*1248A>G ENSP00000286648.5:p.=
ENST00000503359.5:c.*1975A>G ENSP00000426389.1:p.=
ENST00000504730.5:c.*1315A>G ENSP00000425578.1:p.=
ENST00000504952.1:c.*1174A>G ENSP00000421508.1:p.=