Canonical Allele Identifier: CA9206686

Gene: DOCK6 DOCK6-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11208922C>T , CM000681.2:g.11208922C>T	GRCh38
NC_000019.9:g.11319598C>T , CM000681.1:g.11319598C>T	GRCh37
NC_000019.8:g.11180598C>T	NCBI36
NG_031953.1:g.58571G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000587656.6:c.5038G>A (DOCK6)	ENSP00000468638.2:p.Val1680Ile
ENST00000294618.12:c.4933G>A (DOCK6) MANE Select	ENSP00000294618.6:p.Val1645Ile
ENST00000294618.11:c.4933G>A (DOCK6)	ENSP00000294618.6:p.Val1645Ile
ENST00000587656.5:c.2798G>A (DOCK6)
ENST00000588666.1:c.23G>A (DOCK6)
NM_020812.3:c.4933G>A (DOCK6)	NP_065863.2:p.Val1645Ile
XM_005260000.2:c.5131G>A (DOCK6)	XP_005260057.1:p.Val1711Ile
XM_005260001.2:c.5038G>A (DOCK6)	XP_005260058.1:p.Val1680Ile
XM_006722804.2:c.2269G>A (DOCK6)	XP_006722867.1:p.Val757Ile
XM_011528150.1:c.5071G>A (DOCK6)	XP_011526452.1:p.Val1691Ile
XM_011528151.1:c.5059G>A (DOCK6)	XP_011526453.1:p.Val1687Ile
XM_011528152.1:c.4966G>A (DOCK6)	XP_011526454.1:p.Val1656Ile
XR_936195.1:n.5132G>A (DOCK6)
XR_936315.1:n.537+2814C>T (DOCK6-AS1)
NR_134909.1:n.537+2814C>T (DOCK6-AS1)
XM_006722804.3:c.2269G>A (DOCK6)	XP_006722867.1:p.Val757Ile
NM_001367830.1:c.5038G>A (DOCK6)	NP_001354759.1:p.Val1680Ile
NM_020812.4:c.4933G>A (DOCK6) MANE Select	NP_065863.2:p.Val1645Ile