Canonical Allele Identifier: CA9207015

Gene: DOCK6 DOCK6-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11215449C>T , CM000681.2:g.11215449C>T	GRCh38
NC_000019.9:g.11326125C>T , CM000681.1:g.11326125C>T	GRCh37
NC_000019.8:g.11187125C>T	NCBI36
NG_031953.1:g.52044G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_020812.4:c.4044G>A (DOCK6) MANE Select	NP_065863.2:p.Pro1348=
ENST00000294618.12:c.4044G>A (DOCK6) MANE Select	ENSP00000294618.6:p.Pro1348=
NM_001367830.1:c.4149G>A (DOCK6)	NP_001354759.1:p.Pro1383=
NM_020812.3:c.4044G>A (DOCK6)	NP_065863.2:p.Pro1348=
NR_134909.1:n.538-688C>T (DOCK6-AS1)
ENST00000294618.11:c.4044G>A (DOCK6)	ENSP00000294618.6:p.Pro1348=
ENST00000587656.5:c.1909G>A (DOCK6)
ENST00000587656.6:c.4149G>A (DOCK6)	ENSP00000468638.2:p.Pro1383=
XM_005260000.2:c.4242G>A (DOCK6)	XP_005260057.1:p.Pro1414=
XM_005260001.2:c.4149G>A (DOCK6)	XP_005260058.1:p.Pro1383=
XM_006722804.2:c.1380G>A (DOCK6)	XP_006722867.1:p.Pro460=
XM_006722804.3:c.1380G>A (DOCK6)	XP_006722867.1:p.Pro460=
XM_011528150.1:c.4182G>A (DOCK6)	XP_011526452.1:p.Pro1394=
XM_011528151.1:c.4170G>A (DOCK6)	XP_011526453.1:p.Pro1390=
XM_011528152.1:c.4077G>A (DOCK6)	XP_011526454.1:p.Pro1359=
XR_936195.1:n.4243G>A (DOCK6)
XR_936315.1:n.538-688C>T (DOCK6-AS1)