Canonical Allele Identifier: CA2322816766

Gene: DOCK6

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11200725A= , CM000681.2:g.11200725A=	GRCh38
NC_000019.9:g.11311401A= , CM000681.1:g.11311401A=	GRCh37
NC_000019.8:g.11172401A=	NCBI36
NG_031953.1:g.66768T=
NG_051186.1:g.1843T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000587656.6:c.6035T=	ENSP00000468638.2:p.Phe2012=
ENST00000294618.12:c.5930T= MANE Select	ENSP00000294618.6:p.Phe1977=
ENST00000294618.11:c.5930T=	ENSP00000294618.6:p.Phe1977=
ENST00000586702.1:n.833T=
ENST00000587656.5:c.3795T=
ENST00000587734.1:c.75+1164T=	ENSP00000468291.1:n.75+1164T=
NM_020812.3:c.5930T=	NP_065863.2:p.Phe1977=
XM_005260000.2:c.6128T=	XP_005260057.1:p.Phe2043=
XM_005260001.2:c.6035T=	XP_005260058.1:p.Phe2012=
XM_006722804.2:c.3266T=	XP_006722867.1:p.Phe1089=
XM_011528150.1:c.6068T=	XP_011526452.1:p.Phe2023=
XM_011528151.1:c.6056T=	XP_011526453.1:p.Phe2019=
XM_011528152.1:c.5963T=	XP_011526454.1:p.Phe1988=
XR_936195.1:n.6175T=
XM_006722804.3:c.3266T=	XP_006722867.1:p.Phe1089=
NM_001367830.1:c.6035T=	NP_001354759.1:p.Phe2012=
NM_020812.4:c.5930T= MANE Select	NP_065863.2:p.Phe1977=