Canonical Allele Identifier: CA2322816709
Gene: DOCK6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11200613G= , CM000681.2:g.11200613G= GRCh38
NC_000019.9:g.11311289G= , CM000681.1:g.11311289G= GRCh37
NC_000019.8:g.11172289G= NCBI36
NG_031953.1:g.66880C=
NG_051186.1:g.1955C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000587656.6:c.6044+103C= ENSP00000468638.2:n.6044+103C=
ENST00000294618.12:c.5939+103C= MANE Select ENSP00000294618.6:n.5939+103C=
ENST00000294618.11:c.5939+103C= ENSP00000294618.6:n.5939+103C=
ENST00000586702.1:n.842+103C=
ENST00000587656.5:c.3804+103C=
ENST00000587734.1:c.76-1074C= ENSP00000468291.1:n.76-1074C=
NM_020812.3:c.5939+103C= NP_065863.2:n.5939+103C=
XM_005260000.2:c.6137+103C= XP_005260057.1:n.6137+103C=
XM_005260001.2:c.6044+103C= XP_005260058.1:n.6044+103C=
XM_006722804.2:c.3275+103C= XP_006722867.1:n.3275+103C=
XM_011528150.1:c.6077+103C= XP_011526452.1:n.6077+103C=
XM_011528151.1:c.6065+103C= XP_011526453.1:n.6065+103C=
XM_011528152.1:c.5972+103C= XP_011526454.1:n.5972+103C=
XR_936195.1:n.6184+103C=
XM_006722804.3:c.3275+103C= XP_006722867.1:n.3275+103C=
NM_001367830.1:c.6044+103C= NP_001354759.1:n.6044+103C=
NM_020812.4:c.5939+103C= MANE Select NP_065863.2:n.5939+103C=