Canonical Allele Identifier: CA2322826215

Gene: DOCK6

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11220142_11220144delinsCAG , CM000681.2:g.11220142_11220144delinsCAG	GRCh38
NC_000019.9:g.11330818_11330820delinsCAG , CM000681.1:g.11330818_11330820delinsCAG	GRCh37
NC_000019.8:g.11191818_11191820delinsCAG	NCBI36
NG_031953.1:g.47349_47351delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000587656.6:c.3655+1707_3655+1709delinsCTG	ENSP00000468638.2:n.3655+1707_3655+1709delinsCTG
ENST00000294618.12:c.3550+1707_3550+1709delinsCTG MANE Select	ENSP00000294618.6:n.3550+1707_3550+1709delinsCTG
ENST00000294618.11:c.3550+1707_3550+1709delinsCTG	ENSP00000294618.6:n.3550+1707_3550+1709delinsCTG
ENST00000587656.5:c.1415+1707_1415+1709delinsCTG
NM_020812.3:c.3550+1707_3550+1709delinsCTG	NP_065863.2:n.3550+1707_3550+1709delinsCTG
XM_005260000.2:c.3748+1707_3748+1709delinsCTG	XP_005260057.1:n.3748+1707_3748+1709delinsCTG
XM_005260001.2:c.3655+1707_3655+1709delinsCTG	XP_005260058.1:n.3655+1707_3655+1709delinsCTG
XM_006722804.2:c.886+1707_886+1709delinsCTG	XP_006722867.1:n.886+1707_886+1709delinsCTG
XM_011528150.1:c.3688+1707_3688+1709delinsCTG	XP_011526452.1:n.3688+1707_3688+1709delinsCTG
XM_011528151.1:c.3676+1707_3676+1709delinsCTG	XP_011526453.1:n.3676+1707_3676+1709delinsCTG
XM_011528152.1:c.3583+1707_3583+1709delinsCTG	XP_011526454.1:n.3583+1707_3583+1709delinsCTG
XM_011528153.1:c.3688+1707_3688+1709delinsCTG	XP_011526455.1:n.3688+1707_3688+1709delinsCTG
XR_936195.1:n.3749+1707_3749+1709delinsCTG
XR_936196.1:n.3766+1707_3766+1709delinsCTG
XM_006722804.3:c.886+1707_886+1709delinsCTG	XP_006722867.1:n.886+1707_886+1709delinsCTG
NM_001367830.1:c.3655+1707_3655+1709delinsCTG	NP_001354759.1:n.3655+1707_3655+1709delinsCTG
NM_020812.4:c.3550+1707_3550+1709delinsCTG MANE Select	NP_065863.2:n.3550+1707_3550+1709delinsCTG