Canonical Allele Identifier: CA2322816708
Gene: DOCK6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11200610T= , CM000681.2:g.11200610T= GRCh38
NC_000019.9:g.11311286T= , CM000681.1:g.11311286T= GRCh37
NC_000019.8:g.11172286T= NCBI36
NG_031953.1:g.66883A=
NG_051186.1:g.1958A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000587656.6:c.6044+106A= ENSP00000468638.2:n.6044+106A=
ENST00000294618.12:c.5939+106A= MANE Select ENSP00000294618.6:n.5939+106A=
ENST00000294618.11:c.5939+106A= ENSP00000294618.6:n.5939+106A=
ENST00000586702.1:n.842+106A=
ENST00000587656.5:c.3804+106A=
ENST00000587734.1:c.76-1071A= ENSP00000468291.1:n.76-1071A=
NM_020812.3:c.5939+106A= NP_065863.2:n.5939+106A=
XM_005260000.2:c.6137+106A= XP_005260057.1:n.6137+106A=
XM_005260001.2:c.6044+106A= XP_005260058.1:n.6044+106A=
XM_006722804.2:c.3275+106A= XP_006722867.1:n.3275+106A=
XM_011528150.1:c.6077+106A= XP_011526452.1:n.6077+106A=
XM_011528151.1:c.6065+106A= XP_011526453.1:n.6065+106A=
XM_011528152.1:c.5972+106A= XP_011526454.1:n.5972+106A=
XR_936195.1:n.6184+106A=
XM_006722804.3:c.3275+106A= XP_006722867.1:n.3275+106A=
NM_001367830.1:c.6044+106A= NP_001354759.1:n.6044+106A=
NM_020812.4:c.5939+106A= MANE Select NP_065863.2:n.5939+106A=