Canonical Allele Identifier: CA2322824182

Gene: DOCK6 DOCK6-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11215420G= , CM000681.2:g.11215420G=	GRCh38
NC_000019.9:g.11326096G= , CM000681.1:g.11326096G=	GRCh37
NC_000019.8:g.11187096G=	NCBI36
NG_031953.1:g.52073C=

Transcript Alleles

HGVS	Amino-acid Change
NM_020812.4:c.4073C= (DOCK6) MANE Select	NP_065863.2:p.Thr1358=
ENST00000294618.12:c.4073C= (DOCK6) MANE Select	ENSP00000294618.6:p.Thr1358=
NM_001367830.1:c.4178C= (DOCK6)	NP_001354759.1:p.Thr1393=
NM_020812.3:c.4073C= (DOCK6)	NP_065863.2:p.Thr1358=
NR_134909.1:n.538-717G= (DOCK6-AS1)
ENST00000294618.11:c.4073C= (DOCK6)	ENSP00000294618.6:p.Thr1358=
ENST00000587656.5:c.1938C= (DOCK6)
ENST00000587656.6:c.4178C= (DOCK6)	ENSP00000468638.2:p.Thr1393=
XM_005260000.2:c.4271C= (DOCK6)	XP_005260057.1:p.Thr1424=
XM_005260001.2:c.4178C= (DOCK6)	XP_005260058.1:p.Thr1393=
XM_006722804.2:c.1409C= (DOCK6)	XP_006722867.1:p.Thr470=
XM_006722804.3:c.1409C= (DOCK6)	XP_006722867.1:p.Thr470=
XM_011528150.1:c.4211C= (DOCK6)	XP_011526452.1:p.Thr1404=
XM_011528151.1:c.4199C= (DOCK6)	XP_011526453.1:p.Thr1400=
XM_011528152.1:c.4106C= (DOCK6)	XP_011526454.1:p.Thr1369=
XR_936195.1:n.4272C= (DOCK6)
XR_936315.1:n.538-717G= (DOCK6-AS1)