Canonical Allele Identifier: CA9206707

Gene: DOCK6 DOCK6-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11208986C>T , CM000681.2:g.11208986C>T	GRCh38
NC_000019.9:g.11319662C>T , CM000681.1:g.11319662C>T	GRCh37
NC_000019.8:g.11180662C>T	NCBI36
NG_031953.1:g.58507G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000587656.6:c.4974G>A (DOCK6)	ENSP00000468638.2:p.Ala1658=
ENST00000294618.12:c.4869G>A (DOCK6) MANE Select	ENSP00000294618.6:p.Ala1623=
ENST00000294618.11:c.4869G>A (DOCK6)	ENSP00000294618.6:p.Ala1623=
ENST00000587656.5:c.2734G>A (DOCK6)
NM_020812.3:c.4869G>A (DOCK6)	NP_065863.2:p.Ala1623=
XM_005260000.2:c.5067G>A (DOCK6)	XP_005260057.1:p.Ala1689=
XM_005260001.2:c.4974G>A (DOCK6)	XP_005260058.1:p.Ala1658=
XM_006722804.2:c.2205G>A (DOCK6)	XP_006722867.1:p.Ala735=
XM_011528150.1:c.5007G>A (DOCK6)	XP_011526452.1:p.Ala1669=
XM_011528151.1:c.4995G>A (DOCK6)	XP_011526453.1:p.Ala1665=
XM_011528152.1:c.4902G>A (DOCK6)	XP_011526454.1:p.Ala1634=
XR_936195.1:n.5068G>A (DOCK6)
XR_936315.1:n.537+2878C>T (DOCK6-AS1)
NR_134909.1:n.537+2878C>T (DOCK6-AS1)
XM_006722804.3:c.2205G>A (DOCK6)	XP_006722867.1:p.Ala735=
NM_001367830.1:c.4974G>A (DOCK6)	NP_001354759.1:p.Ala1658=
NM_020812.4:c.4869G>A (DOCK6) MANE Select	NP_065863.2:p.Ala1623=