Canonical Allele Identifier: CA1826874079

Gene: DOCK8

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.377145C= , CM000671.2:g.377145C=	GRCh38
NC_000009.11:g.377145C= , CM000671.1:g.377145C=	GRCh37
NC_000009.10:g.367145C=	NCBI36
NG_017007.1:g.167281C= , LRG_196:g.167281C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382329.2:c.2170C=	ENSP00000371766.2:p.Leu724=
ENST00000382331.6:n.871C=
ENST00000483757.6:c.*1061C=	ENSP00000417691.2:n.*1061C=
ENST00000682260.1:n.2270C=
ENST00000685949.1:n.1162C=
ENST00000432829.7:c.2374C= MANE Select	ENSP00000394888.3:p.Leu792=
ENST00000382329.1:c.775C=	ENSP00000371766.1:p.Leu259=
ENST00000382331.5:c.280C=	ENSP00000371768.1:p.Leu94=
ENST00000432829.6:c.2374C=	ENSP00000394888.3:p.Leu792=
ENST00000453981.5:c.2170C=	ENSP00000408464.2:p.Leu724=
ENST00000469391.5:c.2170C=	ENSP00000419438.1:p.Leu724=
ENST00000483757.5:c.*1849C=	ENSP00000417691.1:n.*1849C=
ENST00000495184.5:n.4329C=
NM_001190458.1:c.2170C=	NP_001177387.1:p.Leu724=
NM_001193536.1:c.2170C=	NP_001180465.1:p.Leu724=
NM_203447.3:c.2374C= , LRG_196t1:c.2374C=	NP_982272.2:p.Leu792=
XM_011518045.1:c.2170C=	XP_011516347.1:p.Leu724=
XM_011518046.1:c.2236C=	XP_011516348.1:p.Leu746=
XM_011518047.1:c.2170C=	XP_011516349.1:p.Leu724=
XM_011518048.1:c.2170C=	XP_011516350.1:p.Leu724=
XM_011518049.1:c.610C=	XP_011516351.1:p.Leu204=
XM_011518045.3:c.2170C=	XP_011516347.1:p.Leu724=
XM_011518046.2:c.2236C=	XP_011516348.1:p.Leu746=
XM_011518047.3:c.2170C=	XP_011516349.1:p.Leu724=
XM_011518048.2:c.2170C=	XP_011516350.1:p.Leu724=
XM_011518049.2:c.610C=	XP_011516351.1:p.Leu204=
XM_017015173.1:c.2170C=	XP_016870662.1:p.Leu724=
XM_017015174.1:c.2236C=	XP_016870663.1:p.Leu746=
NM_001190458.2:c.2170C=	NP_001177387.1:p.Leu724=
NM_001193536.2:c.2170C=	NP_001180465.1:p.Leu724=
NM_203447.4:c.2374C= MANE Select	NP_982272.2:p.Leu792=