Canonical Allele Identifier: CA2962595724

Gene: DOCK6 DOCK6-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11215533del , CM000681.2:g.11215533del	GRCh38
NC_000019.9:g.11326209del , CM000681.1:g.11326209del	GRCh37
NC_000019.8:g.11187209del	NCBI36
NG_031953.1:g.51961del

Transcript Alleles

HGVS	Amino-acid Change
NM_020812.4:c.4022-61del (DOCK6) MANE Select	NP_065863.2:n.4022-61del
ENST00000294618.12:c.4022-61del (DOCK6) MANE Select	ENSP00000294618.6:n.4022-61del
NM_001367830.1:c.4127-61del (DOCK6)	NP_001354759.1:n.4127-61del
NM_020812.3:c.4022-61del (DOCK6)	NP_065863.2:n.4022-61del
NR_134909.1:n.538-604del (DOCK6-AS1)
ENST00000294618.11:c.4022-61del (DOCK6)	ENSP00000294618.6:n.4022-61del
ENST00000587656.5:c.1887-61del (DOCK6)
ENST00000587656.6:c.4127-61del (DOCK6)	ENSP00000468638.2:n.4127-61del
XM_005260000.2:c.4220-61del (DOCK6)	XP_005260057.1:n.4220-61del
XM_005260001.2:c.4127-61del (DOCK6)	XP_005260058.1:n.4127-61del
XM_006722804.2:c.1358-61del (DOCK6)	XP_006722867.1:n.1358-61del
XM_006722804.3:c.1358-61del (DOCK6)	XP_006722867.1:n.1358-61del
XM_011528150.1:c.4160-61del (DOCK6)	XP_011526452.1:n.4160-61del
XM_011528151.1:c.4148-61del (DOCK6)	XP_011526453.1:n.4148-61del
XM_011528152.1:c.4055-61del (DOCK6)	XP_011526454.1:n.4055-61del
XM_011528153.1:c.4227del (DOCK6)	XP_011526455.1:p.Ter1410AspextTer?
XR_936195.1:n.4221-61del (DOCK6)
XR_936315.1:n.538-604del (DOCK6-AS1)