Canonical Allele Identifier: CA2322831914

Gene: DOCK6

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11232035A= , CM000681.2:g.11232035A=	GRCh38
NC_000019.9:g.11342711A= , CM000681.1:g.11342711A=	GRCh37
NC_000019.8:g.11203711A=	NCBI36
NG_031953.1:g.35458T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000587656.6:c.2823+150T=	ENSP00000468638.2:n.2823+150T=
ENST00000294618.12:c.2718+1168T= MANE Select	ENSP00000294618.6:n.2718+1168T=
ENST00000294618.11:c.2718+1168T=	ENSP00000294618.6:n.2718+1168T=
ENST00000585904.1:c.426+150T=	ENSP00000465767.1:n.426+150T=
ENST00000587656.5:c.583+150T=
ENST00000590680.5:c.1061+1168T=
NM_020812.3:c.2718+1168T=	NP_065863.2:n.2718+1168T=
XM_005260000.2:c.2823+150T=	XP_005260057.1:n.2823+150T=
XM_005260001.2:c.2823+150T=	XP_005260058.1:n.2823+150T=
XM_006722804.2:c.54+1004T=	XP_006722867.1:n.54+1004T=
XM_011528150.1:c.2856+150T=	XP_011526452.1:n.2856+150T=
XM_011528151.1:c.2751+1168T=	XP_011526453.1:n.2751+1168T=
XM_011528152.1:c.2751+1168T=	XP_011526454.1:n.2751+1168T=
XM_011528153.1:c.2856+150T=	XP_011526455.1:n.2856+150T=
XR_936195.1:n.2917+150T=
XR_936196.1:n.2812+1168T=
XR_936197.1:n.2917+150T=
XR_936198.1:n.2812+1168T=
XM_006722804.3:c.54+1004T=	XP_006722867.1:n.54+1004T=
NM_001367830.1:c.2823+150T=	NP_001354759.1:n.2823+150T=
NM_020812.4:c.2718+1168T= MANE Select	NP_065863.2:n.2718+1168T=