Canonical Allele Identifier: CA781922699
Gene: DOK6 HGNC NCBI

Linked Data

dbSNP Id: rs1166903331

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.69615926T>A , CM000680.2:g.69615926T>A GRCh38
NC_000018.9:g.67283162T>A , CM000680.1:g.67283162T>A GRCh37
NC_000018.8:g.65434142T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000382713.10:c.289+16428T>A MANE Select ENSP00000372160.5:n.289+16428T>A
ENST00000382713.9:c.289+16428T>A ENSP00000372160.5:n.289+16428T>A
NM_152721.5:c.289+16428T>A NP_689934.2:n.289+16428T>A
XM_011525873.1:c.289+16428T>A XP_011524175.1:n.289+16428T>A
XM_011525874.1:c.289+16428T>A XP_011524176.1:n.289+16428T>A
XM_011525875.1:c.289+16428T>A XP_011524177.1:n.289+16428T>A
XM_011525875.2:c.289+16428T>A XP_011524177.1:n.289+16428T>A
NM_152721.6:c.289+16428T>A MANE Select NP_689934.2:n.289+16428T>A