Canonical Allele Identifier: CA9206929

Gene: DOCK6 DOCK6-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11214408G>A , CM000681.2:g.11214408G>A	GRCh38
NC_000019.9:g.11325084G>A , CM000681.1:g.11325084G>A	GRCh37
NC_000019.8:g.11186084G>A	NCBI36
NG_031953.1:g.53085C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_020812.4:c.4205C>T (DOCK6) MANE Select	NP_065863.2:p.Thr1402Met
ENST00000294618.12:c.4205C>T (DOCK6) MANE Select	ENSP00000294618.6:p.Thr1402Met
NM_001367830.1:c.4310C>T (DOCK6)	NP_001354759.1:p.Thr1437Met
NM_020812.3:c.4205C>T (DOCK6)	NP_065863.2:p.Thr1402Met
NR_134909.1:n.538-1729G>A (DOCK6-AS1)
ENST00000294618.11:c.4205C>T (DOCK6)	ENSP00000294618.6:p.Thr1402Met
ENST00000587656.5:c.2070C>T (DOCK6)
ENST00000587656.6:c.4310C>T (DOCK6)	ENSP00000468638.2:p.Thr1437Met
XM_005260000.2:c.4403C>T (DOCK6)	XP_005260057.1:p.Thr1468Met
XM_005260001.2:c.4310C>T (DOCK6)	XP_005260058.1:p.Thr1437Met
XM_006722804.2:c.1541C>T (DOCK6)	XP_006722867.1:p.Thr514Met
XM_006722804.3:c.1541C>T (DOCK6)	XP_006722867.1:p.Thr514Met
XM_011528150.1:c.4343C>T (DOCK6)	XP_011526452.1:p.Thr1448Met
XM_011528151.1:c.4331C>T (DOCK6)	XP_011526453.1:p.Thr1444Met
XM_011528152.1:c.4238C>T (DOCK6)	XP_011526454.1:p.Thr1413Met
XR_936195.1:n.4404C>T (DOCK6)
XR_936315.1:n.538-1729G>A (DOCK6-AS1)