Canonical Allele Identifier: CA1826902218

Gene: DOCK8

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.441358C= , CM000671.2:g.441358C=	GRCh38
NC_000009.11:g.441358C= , CM000671.1:g.441358C=	GRCh37
NC_000009.10:g.431358C=	NCBI36
NG_017007.1:g.231494C= , LRG_196:g.231494C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000382329.2:c.4996C=	ENSP00000371766.2:p.Arg1666=
ENST00000683406.1:n.1771C=
ENST00000684637.1:n.977C=
ENST00000685949.1:n.4084C=
ENST00000432829.7:c.5296C= MANE Select	ENSP00000394888.3:p.Arg1766=
ENST00000382329.1:c.3697C=	ENSP00000371766.1:p.Arg1233=
ENST00000432829.6:c.5296C=	ENSP00000394888.3:p.Arg1766=
ENST00000453981.5:c.5092C=	ENSP00000408464.2:p.Arg1698=
ENST00000469391.5:c.4996C=	ENSP00000419438.1:p.Arg1666=
ENST00000495184.5:n.7251C=
NM_001190458.1:c.4996C=	NP_001177387.1:p.Arg1666=
NM_001193536.1:c.5092C=	NP_001180465.1:p.Arg1698=
NM_203447.3:c.5296C= , LRG_196t1:c.5296C=	NP_982272.2:p.Arg1766=
XM_011518045.1:c.4996C=	XP_011516347.1:p.Arg1666=
XM_011518046.1:c.5158C=	XP_011516348.1:p.Arg1720=
XM_011518047.1:c.5092C=	XP_011516349.1:p.Arg1698=
XM_011518048.1:c.5092C=	XP_011516350.1:p.Arg1698=
XM_011518049.1:c.3532C=	XP_011516351.1:p.Arg1178=
XM_011518045.3:c.4996C=	XP_011516347.1:p.Arg1666=
XM_011518046.2:c.5158C=	XP_011516348.1:p.Arg1720=
XM_011518047.3:c.5092C=	XP_011516349.1:p.Arg1698=
XM_011518048.2:c.5092C=	XP_011516350.1:p.Arg1698=
XM_011518049.2:c.3532C=	XP_011516351.1:p.Arg1178=
XM_017015173.1:c.5092C=	XP_016870662.1:p.Arg1698=
XM_017015174.1:c.5158C=	XP_016870663.1:p.Arg1720=
NM_001190458.2:c.4996C=	NP_001177387.1:p.Arg1666=
NM_001193536.2:c.5092C=	NP_001180465.1:p.Arg1698=
NM_203447.4:c.5296C= MANE Select	NP_982272.2:p.Arg1766=