Canonical Allele Identifier: CA14730316

Gene: DOCK6 DOCK6-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11212995C>T , CM000681.2:g.11212995C>T	GRCh38
NC_000019.9:g.11323671C>T , CM000681.1:g.11323671C>T	GRCh37
NC_000019.8:g.11184671C>T	NCBI36
NG_031953.1:g.54498G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_020812.4:c.4491+181G>A (DOCK6) MANE Select	NP_065863.2:n.4491+181G>A
ENST00000294618.12:c.4491+181G>A (DOCK6) MANE Select	ENSP00000294618.6:n.4491+181G>A
NM_001367830.1:c.4596+181G>A (DOCK6)	NP_001354759.1:n.4596+181G>A
NM_020812.3:c.4491+181G>A (DOCK6)	NP_065863.2:n.4491+181G>A
NR_134909.1:n.538-3142C>T (DOCK6-AS1)
ENST00000294618.11:c.4491+181G>A (DOCK6)	ENSP00000294618.6:n.4491+181G>A
ENST00000587656.5:c.2356+181G>A (DOCK6)
ENST00000587656.6:c.4596+181G>A (DOCK6)	ENSP00000468638.2:n.4596+181G>A
XM_005260000.2:c.4689+181G>A (DOCK6)	XP_005260057.1:n.4689+181G>A
XM_005260001.2:c.4596+181G>A (DOCK6)	XP_005260058.1:n.4596+181G>A
XM_006722804.2:c.1827+181G>A (DOCK6)	XP_006722867.1:n.1827+181G>A
XM_006722804.3:c.1827+181G>A (DOCK6)	XP_006722867.1:n.1827+181G>A
XM_011528150.1:c.4629+181G>A (DOCK6)	XP_011526452.1:n.4629+181G>A
XM_011528151.1:c.4617+181G>A (DOCK6)	XP_011526453.1:n.4617+181G>A
XM_011528152.1:c.4524+181G>A (DOCK6)	XP_011526454.1:n.4524+181G>A
XR_936195.1:n.4690+181G>A (DOCK6)
XR_936315.1:n.538-3142C>T (DOCK6-AS1)