Canonical Allele Identifier: CA2322816764

Gene: DOCK6

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11200722C= , CM000681.2:g.11200722C=	GRCh38
NC_000019.9:g.11311398C= , CM000681.1:g.11311398C=	GRCh37
NC_000019.8:g.11172398C=	NCBI36
NG_031953.1:g.66771G=
NG_051186.1:g.1846G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000587656.6:c.6038G=	ENSP00000468638.2:p.Cys2013=
ENST00000294618.12:c.5933G= MANE Select	ENSP00000294618.6:p.Cys1978=
ENST00000294618.11:c.5933G=	ENSP00000294618.6:p.Cys1978=
ENST00000586702.1:n.836G=
ENST00000587656.5:c.3798G=
ENST00000587734.1:c.75+1167G=	ENSP00000468291.1:n.75+1167G=
NM_020812.3:c.5933G=	NP_065863.2:p.Cys1978=
XM_005260000.2:c.6131G=	XP_005260057.1:p.Cys2044=
XM_005260001.2:c.6038G=	XP_005260058.1:p.Cys2013=
XM_006722804.2:c.3269G=	XP_006722867.1:p.Cys1090=
XM_011528150.1:c.6071G=	XP_011526452.1:p.Cys2024=
XM_011528151.1:c.6059G=	XP_011526453.1:p.Cys2020=
XM_011528152.1:c.5966G=	XP_011526454.1:p.Cys1989=
XR_936195.1:n.6178G=
XM_006722804.3:c.3269G=	XP_006722867.1:p.Cys1090=
NM_001367830.1:c.6038G=	NP_001354759.1:p.Cys2013=
NM_020812.4:c.5933G= MANE Select	NP_065863.2:p.Cys1978=