Canonical Allele Identifier: CA2322832027

Gene: DOCK6

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11232278G= , CM000681.2:g.11232278G=	GRCh38
NC_000019.9:g.11342954G= , CM000681.1:g.11342954G=	GRCh37
NC_000019.8:g.11203954G=	NCBI36
NG_031953.1:g.35215C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000587656.6:c.2730C=	ENSP00000468638.2:p.Arg910=
ENST00000294618.12:c.2718+925C= MANE Select	ENSP00000294618.6:n.2718+925C=
ENST00000294618.11:c.2718+925C=	ENSP00000294618.6:n.2718+925C=
ENST00000585904.1:c.333C=	ENSP00000465767.1:p.Arg111=
ENST00000587656.5:c.490C=
ENST00000590680.5:c.1061+925C=
NM_020812.3:c.2718+925C=	NP_065863.2:n.2718+925C=
XM_005260000.2:c.2730C=	XP_005260057.1:p.Arg910=
XM_005260001.2:c.2730C=	XP_005260058.1:p.Arg910=
XM_006722804.2:c.54+761C=	XP_006722867.1:n.54+761C=
XM_011528150.1:c.2763C=	XP_011526452.1:p.Arg921=
XM_011528151.1:c.2751+925C=	XP_011526453.1:n.2751+925C=
XM_011528152.1:c.2751+925C=	XP_011526454.1:n.2751+925C=
XM_011528153.1:c.2763C=	XP_011526455.1:p.Arg921=
XR_936195.1:n.2824C=
XR_936196.1:n.2812+925C=
XR_936197.1:n.2824C=
XR_936198.1:n.2812+925C=
XM_006722804.3:c.54+761C=	XP_006722867.1:n.54+761C=
NM_001367830.1:c.2730C=	NP_001354759.1:p.Arg910=
NM_020812.4:c.2718+925C= MANE Select	NP_065863.2:n.2718+925C=