Canonical Allele Identifier: CA1826874092

Gene: DOCK8

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.377168C= , CM000671.2:g.377168C=	GRCh38
NC_000009.11:g.377168C= , CM000671.1:g.377168C=	GRCh37
NC_000009.10:g.367168C=	NCBI36
NG_017007.1:g.167304C= , LRG_196:g.167304C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382329.2:c.2193C=	ENSP00000371766.2:p.Leu731=
ENST00000382331.6:n.894C=
ENST00000483757.6:c.*1084C=	ENSP00000417691.2:n.*1084C=
ENST00000682260.1:n.2293C=
ENST00000685949.1:n.1185C=
ENST00000432829.7:c.2397C= MANE Select	ENSP00000394888.3:p.Leu799=
ENST00000382329.1:c.798C=	ENSP00000371766.1:p.Leu266=
ENST00000382331.5:c.303C=	ENSP00000371768.1:p.Leu101=
ENST00000432829.6:c.2397C=	ENSP00000394888.3:p.Leu799=
ENST00000453981.5:c.2193C=	ENSP00000408464.2:p.Leu731=
ENST00000469391.5:c.2193C=	ENSP00000419438.1:p.Leu731=
ENST00000483757.5:c.*1872C=	ENSP00000417691.1:n.*1872C=
ENST00000495184.5:n.4352C=
NM_001190458.1:c.2193C=	NP_001177387.1:p.Leu731=
NM_001193536.1:c.2193C=	NP_001180465.1:p.Leu731=
NM_203447.3:c.2397C= , LRG_196t1:c.2397C=	NP_982272.2:p.Leu799=
XM_011518045.1:c.2193C=	XP_011516347.1:p.Leu731=
XM_011518046.1:c.2259C=	XP_011516348.1:p.Leu753=
XM_011518047.1:c.2193C=	XP_011516349.1:p.Leu731=
XM_011518048.1:c.2193C=	XP_011516350.1:p.Leu731=
XM_011518049.1:c.633C=	XP_011516351.1:p.Leu211=
XM_011518045.3:c.2193C=	XP_011516347.1:p.Leu731=
XM_011518046.2:c.2259C=	XP_011516348.1:p.Leu753=
XM_011518047.3:c.2193C=	XP_011516349.1:p.Leu731=
XM_011518048.2:c.2193C=	XP_011516350.1:p.Leu731=
XM_011518049.2:c.633C=	XP_011516351.1:p.Leu211=
XM_017015173.1:c.2193C=	XP_016870662.1:p.Leu731=
XM_017015174.1:c.2259C=	XP_016870663.1:p.Leu753=
NM_001190458.2:c.2193C=	NP_001177387.1:p.Leu731=
NM_001193536.2:c.2193C=	NP_001180465.1:p.Leu731=
NM_203447.4:c.2397C= MANE Select	NP_982272.2:p.Leu799=