Canonical Allele Identifier: CA2322816758

Gene: DOCK6

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11200712C= , CM000681.2:g.11200712C=	GRCh38
NC_000019.9:g.11311388C= , CM000681.1:g.11311388C=	GRCh37
NC_000019.8:g.11172388C=	NCBI36
NG_031953.1:g.66781G=
NG_051186.1:g.1856G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000587656.6:c.6044+4G=	ENSP00000468638.2:n.6044+4G=
ENST00000294618.12:c.5939+4G= MANE Select	ENSP00000294618.6:n.5939+4G=
ENST00000294618.11:c.5939+4G=	ENSP00000294618.6:n.5939+4G=
ENST00000586702.1:n.842+4G=
ENST00000587656.5:c.3804+4G=
ENST00000587734.1:c.76-1173G=	ENSP00000468291.1:n.76-1173G=
NM_020812.3:c.5939+4G=	NP_065863.2:n.5939+4G=
XM_005260000.2:c.6137+4G=	XP_005260057.1:n.6137+4G=
XM_005260001.2:c.6044+4G=	XP_005260058.1:n.6044+4G=
XM_006722804.2:c.3275+4G=	XP_006722867.1:n.3275+4G=
XM_011528150.1:c.6077+4G=	XP_011526452.1:n.6077+4G=
XM_011528151.1:c.6065+4G=	XP_011526453.1:n.6065+4G=
XM_011528152.1:c.5972+4G=	XP_011526454.1:n.5972+4G=
XR_936195.1:n.6184+4G=
XM_006722804.3:c.3275+4G=	XP_006722867.1:n.3275+4G=
NM_001367830.1:c.6044+4G=	NP_001354759.1:n.6044+4G=
NM_020812.4:c.5939+4G= MANE Select	NP_065863.2:n.5939+4G=