Canonical Allele Identifier: CA9206697
Gene: DOCK6 HGNC NCBI
DOCK6-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11208956C>T , CM000681.2:g.11208956C>T GRCh38
NC_000019.9:g.11319632C>T , CM000681.1:g.11319632C>T GRCh37
NC_000019.8:g.11180632C>T NCBI36
NG_031953.1:g.58537G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000587656.6:c.5004G>A (DOCK6) ENSP00000468638.2:p.Leu1668=
ENST00000294618.12:c.4899G>A (DOCK6) MANE Select ENSP00000294618.6:p.Leu1633=
ENST00000294618.11:c.4899G>A (DOCK6) ENSP00000294618.6:p.Leu1633=
ENST00000587656.5:c.2764G>A (DOCK6)
NM_020812.3:c.4899G>A (DOCK6) NP_065863.2:p.Leu1633=
XM_005260000.2:c.5097G>A (DOCK6) XP_005260057.1:p.Leu1699=
XM_005260001.2:c.5004G>A (DOCK6) XP_005260058.1:p.Leu1668=
XM_006722804.2:c.2235G>A (DOCK6) XP_006722867.1:p.Leu745=
XM_011528150.1:c.5037G>A (DOCK6) XP_011526452.1:p.Leu1679=
XM_011528151.1:c.5025G>A (DOCK6) XP_011526453.1:p.Leu1675=
XM_011528152.1:c.4932G>A (DOCK6) XP_011526454.1:p.Leu1644=
XR_936195.1:n.5098G>A (DOCK6)
XR_936315.1:n.537+2848C>T (DOCK6-AS1)
NR_134909.1:n.537+2848C>T (DOCK6-AS1)
XM_006722804.3:c.2235G>A (DOCK6) XP_006722867.1:p.Leu745=
NM_001367830.1:c.5004G>A (DOCK6) NP_001354759.1:p.Leu1668=
NM_020812.4:c.4899G>A (DOCK6) MANE Select NP_065863.2:p.Leu1633=