Canonical Allele Identifier: CA2322832022

Gene: DOCK6

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11232264A= , CM000681.2:g.11232264A=	GRCh38
NC_000019.9:g.11342940A= , CM000681.1:g.11342940A=	GRCh37
NC_000019.8:g.11203940A=	NCBI36
NG_031953.1:g.35229T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000587656.6:c.2744T=	ENSP00000468638.2:p.Val915=
ENST00000294618.12:c.2718+939T= MANE Select	ENSP00000294618.6:n.2718+939T=
ENST00000294618.11:c.2718+939T=	ENSP00000294618.6:n.2718+939T=
ENST00000585904.1:c.347T=	ENSP00000465767.1:p.Val116=
ENST00000587656.5:c.504T=
ENST00000590680.5:c.1061+939T=
NM_020812.3:c.2718+939T=	NP_065863.2:n.2718+939T=
XM_005260000.2:c.2744T=	XP_005260057.1:p.Val915=
XM_005260001.2:c.2744T=	XP_005260058.1:p.Val915=
XM_006722804.2:c.54+775T=	XP_006722867.1:n.54+775T=
XM_011528150.1:c.2777T=	XP_011526452.1:p.Val926=
XM_011528151.1:c.2751+939T=	XP_011526453.1:n.2751+939T=
XM_011528152.1:c.2751+939T=	XP_011526454.1:n.2751+939T=
XM_011528153.1:c.2777T=	XP_011526455.1:p.Val926=
XR_936195.1:n.2838T=
XR_936196.1:n.2812+939T=
XR_936197.1:n.2838T=
XR_936198.1:n.2812+939T=
XM_006722804.3:c.54+775T=	XP_006722867.1:n.54+775T=
NM_001367830.1:c.2744T=	NP_001354759.1:p.Val915=
NM_020812.4:c.2718+939T= MANE Select	NP_065863.2:n.2718+939T=