Canonical Allele Identifier: CA305311068

Gene: DOCK6 DOCK6-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11213515C>A , CM000681.2:g.11213515C>A	GRCh38
NC_000019.9:g.11324191C>A , CM000681.1:g.11324191C>A	GRCh37
NC_000019.8:g.11185191C>A	NCBI36
NG_031953.1:g.53978G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000587656.6:c.4444-187G>T (DOCK6)	ENSP00000468638.2:n.4444-187G>T
ENST00000294618.12:c.4339-187G>T (DOCK6) MANE Select	ENSP00000294618.6:n.4339-187G>T
ENST00000294618.11:c.4339-187G>T (DOCK6)	ENSP00000294618.6:n.4339-187G>T
ENST00000587656.5:c.2204-187G>T (DOCK6)
NM_020812.3:c.4339-187G>T (DOCK6)	NP_065863.2:n.4339-187G>T
XM_005260000.2:c.4537-187G>T (DOCK6)	XP_005260057.1:n.4537-187G>T
XM_005260001.2:c.4444-187G>T (DOCK6)	XP_005260058.1:n.4444-187G>T
XM_006722804.2:c.1675-187G>T (DOCK6)	XP_006722867.1:n.1675-187G>T
XM_011528150.1:c.4477-187G>T (DOCK6)	XP_011526452.1:n.4477-187G>T
XM_011528151.1:c.4465-187G>T (DOCK6)	XP_011526453.1:n.4465-187G>T
XM_011528152.1:c.4372-187G>T (DOCK6)	XP_011526454.1:n.4372-187G>T
XR_936195.1:n.4538-187G>T (DOCK6)
XR_936315.1:n.538-2622C>A (DOCK6-AS1)
NR_134909.1:n.538-2622C>A (DOCK6-AS1)
XM_006722804.3:c.1675-187G>T (DOCK6)	XP_006722867.1:n.1675-187G>T
NM_001367830.1:c.4444-187G>T (DOCK6)	NP_001354759.1:n.4444-187G>T
NM_020812.4:c.4339-187G>T (DOCK6) MANE Select	NP_065863.2:n.4339-187G>T