Canonical Allele Identifier: CA9206623

Gene: DOCK6 DOCK6-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11204328C>T , CM000681.2:g.11204328C>T	GRCh38
NC_000019.9:g.11315004C>T , CM000681.1:g.11315004C>T	GRCh37
NC_000019.8:g.11176004C>T	NCBI36
NG_031953.1:g.63165G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000587656.6:c.5197G>A (DOCK6)	ENSP00000468638.2:p.Gly1733Arg
ENST00000294618.12:c.5092G>A (DOCK6) MANE Select	ENSP00000294618.6:p.Gly1698Arg
ENST00000294618.11:c.5092G>A (DOCK6)	ENSP00000294618.6:p.Gly1698Arg
ENST00000587656.5:c.2957G>A (DOCK6)
ENST00000588666.1:c.179-1613G>A (DOCK6)
NM_020812.3:c.5092G>A (DOCK6)	NP_065863.2:p.Gly1698Arg
XM_005260000.2:c.5290G>A (DOCK6)	XP_005260057.1:p.Gly1764Arg
XM_005260001.2:c.5197G>A (DOCK6)	XP_005260058.1:p.Gly1733Arg
XM_006722804.2:c.2428G>A (DOCK6)	XP_006722867.1:p.Gly810Arg
XM_011528150.1:c.5230G>A (DOCK6)	XP_011526452.1:p.Gly1744Arg
XM_011528151.1:c.5218G>A (DOCK6)	XP_011526453.1:p.Gly1740Arg
XM_011528152.1:c.5125G>A (DOCK6)	XP_011526454.1:p.Gly1709Arg
XR_936195.1:n.5291G>A (DOCK6)
XR_936315.1:n.238+463C>T (DOCK6-AS1)
NR_134909.1:n.238+463C>T (DOCK6-AS1)
XM_006722804.3:c.2428G>A (DOCK6)	XP_006722867.1:p.Gly810Arg
NM_001367830.1:c.5197G>A (DOCK6)	NP_001354759.1:p.Gly1733Arg
NM_020812.4:c.5092G>A (DOCK6) MANE Select	NP_065863.2:p.Gly1698Arg