Canonical Allele Identifier: CA2322816763

Gene: DOCK6

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11200721G= , CM000681.2:g.11200721G=	GRCh38
NC_000019.9:g.11311397G= , CM000681.1:g.11311397G=	GRCh37
NC_000019.8:g.11172397G=	NCBI36
NG_031953.1:g.66772C=
NG_051186.1:g.1847C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000587656.6:c.6039C=	ENSP00000468638.2:p.Cys2013=
ENST00000294618.12:c.5934C= MANE Select	ENSP00000294618.6:p.Cys1978=
ENST00000294618.11:c.5934C=	ENSP00000294618.6:p.Cys1978=
ENST00000586702.1:n.837C=
ENST00000587656.5:c.3799C=
ENST00000587734.1:c.75+1168C=	ENSP00000468291.1:n.75+1168C=
NM_020812.3:c.5934C=	NP_065863.2:p.Cys1978=
XM_005260000.2:c.6132C=	XP_005260057.1:p.Cys2044=
XM_005260001.2:c.6039C=	XP_005260058.1:p.Cys2013=
XM_006722804.2:c.3270C=	XP_006722867.1:p.Cys1090=
XM_011528150.1:c.6072C=	XP_011526452.1:p.Cys2024=
XM_011528151.1:c.6060C=	XP_011526453.1:p.Cys2020=
XM_011528152.1:c.5967C=	XP_011526454.1:p.Cys1989=
XR_936195.1:n.6179C=
XM_006722804.3:c.3270C=	XP_006722867.1:p.Cys1090=
NM_001367830.1:c.6039C=	NP_001354759.1:p.Cys2013=
NM_020812.4:c.5934C= MANE Select	NP_065863.2:p.Cys1978=