Canonical Allele Identifier: CA2322816762
Gene: DOCK6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11200719T= , CM000681.2:g.11200719T= GRCh38
NC_000019.9:g.11311395T= , CM000681.1:g.11311395T= GRCh37
NC_000019.8:g.11172395T= NCBI36
NG_031953.1:g.66774A=
NG_051186.1:g.1849A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000587656.6:c.6041A= ENSP00000468638.2:p.Lys2014=
ENST00000294618.12:c.5936A= MANE Select ENSP00000294618.6:p.Lys1979=
ENST00000294618.11:c.5936A= ENSP00000294618.6:p.Lys1979=
ENST00000586702.1:n.839A=
ENST00000587656.5:c.3801A=
ENST00000587734.1:c.75+1170A= ENSP00000468291.1:n.75+1170A=
NM_020812.3:c.5936A= NP_065863.2:p.Lys1979=
XM_005260000.2:c.6134A= XP_005260057.1:p.Lys2045=
XM_005260001.2:c.6041A= XP_005260058.1:p.Lys2014=
XM_006722804.2:c.3272A= XP_006722867.1:p.Lys1091=
XM_011528150.1:c.6074A= XP_011526452.1:p.Lys2025=
XM_011528151.1:c.6062A= XP_011526453.1:p.Lys2021=
XM_011528152.1:c.5969A= XP_011526454.1:p.Lys1990=
XR_936195.1:n.6181A=
XM_006722804.3:c.3272A= XP_006722867.1:p.Lys1091=
NM_001367830.1:c.6041A= NP_001354759.1:p.Lys2014=
NM_020812.4:c.5936A= MANE Select NP_065863.2:p.Lys1979=