Canonical Allele Identifier: CA9206665
Gene: DOCK6 HGNC NCBI
DOCK6-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11208815G>A , CM000681.2:g.11208815G>A GRCh38
NC_000019.9:g.11319491G>A , CM000681.1:g.11319491G>A GRCh37
NC_000019.8:g.11180491G>A NCBI36
NG_031953.1:g.58678C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000587656.6:c.5064C>T (DOCK6) ENSP00000468638.2:p.Asn1688=
ENST00000294618.12:c.4959C>T (DOCK6) MANE Select ENSP00000294618.6:p.Asn1653=
ENST00000294618.11:c.4959C>T (DOCK6) ENSP00000294618.6:p.Asn1653=
ENST00000587656.5:c.2824C>T (DOCK6)
ENST00000588666.1:c.49C>T (DOCK6)
NM_020812.3:c.4959C>T (DOCK6) NP_065863.2:p.Asn1653=
XM_005260000.2:c.5157C>T (DOCK6) XP_005260057.1:p.Asn1719=
XM_005260001.2:c.5064C>T (DOCK6) XP_005260058.1:p.Asn1688=
XM_006722804.2:c.2295C>T (DOCK6) XP_006722867.1:p.Asn765=
XM_011528150.1:c.5097C>T (DOCK6) XP_011526452.1:p.Asn1699=
XM_011528151.1:c.5085C>T (DOCK6) XP_011526453.1:p.Asn1695=
XM_011528152.1:c.4992C>T (DOCK6) XP_011526454.1:p.Asn1664=
XR_936195.1:n.5158C>T (DOCK6)
XR_936315.1:n.537+2707G>A (DOCK6-AS1)
NR_134909.1:n.537+2707G>A (DOCK6-AS1)
XM_006722804.3:c.2295C>T (DOCK6) XP_006722867.1:p.Asn765=
NM_001367830.1:c.5064C>T (DOCK6) NP_001354759.1:p.Asn1688=
NM_020812.4:c.4959C>T (DOCK6) MANE Select NP_065863.2:p.Asn1653=