Canonical Allele Identifier: CA404069714
Gene: DOCK6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11200720T>G , CM000681.2:g.11200720T>G GRCh38
NC_000019.9:g.11311396T>G , CM000681.1:g.11311396T>G GRCh37
NC_000019.8:g.11172396T>G NCBI36
NG_031953.1:g.66773A>C
NG_051186.1:g.1848A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000587656.6:c.6040A>C ENSP00000468638.2:p.Lys2014Gln
ENST00000294618.12:c.5935A>C MANE Select ENSP00000294618.6:p.Lys1979Gln
ENST00000294618.11:c.5935A>C ENSP00000294618.6:p.Lys1979Gln
ENST00000586702.1:n.838A>C
ENST00000587656.5:c.3800A>C
ENST00000587734.1:c.75+1169A>C ENSP00000468291.1:n.75+1169A>C
NM_020812.3:c.5935A>C NP_065863.2:p.Lys1979Gln
XM_005260000.2:c.6133A>C XP_005260057.1:p.Lys2045Gln
XM_005260001.2:c.6040A>C XP_005260058.1:p.Lys2014Gln
XM_006722804.2:c.3271A>C XP_006722867.1:p.Lys1091Gln
XM_011528150.1:c.6073A>C XP_011526452.1:p.Lys2025Gln
XM_011528151.1:c.6061A>C XP_011526453.1:p.Lys2021Gln
XM_011528152.1:c.5968A>C XP_011526454.1:p.Lys1990Gln
XR_936195.1:n.6180A>C
XM_006722804.3:c.3271A>C XP_006722867.1:p.Lys1091Gln
NM_001367830.1:c.6040A>C NP_001354759.1:p.Lys2014Gln
NM_020812.4:c.5935A>C MANE Select NP_065863.2:p.Lys1979Gln