Canonical Allele Identifier: CA1826891847

Gene: DOCK8

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.418090C= , CM000671.2:g.418090C=	GRCh38
NC_000009.11:g.418090C= , CM000671.1:g.418090C=	GRCh37
NC_000009.10:g.408090C=	NCBI36
NG_017007.1:g.208226C= , LRG_196:g.208226C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000382329.2:c.3423C=	ENSP00000371766.2:p.Arg1141=
ENST00000683406.1:n.244C=
ENST00000685949.1:n.2511C=
ENST00000432829.7:c.3723C= MANE Select	ENSP00000394888.3:p.Arg1241=
ENST00000382329.1:c.2124C=	ENSP00000371766.1:p.Arg708=
ENST00000432829.6:c.3723C=	ENSP00000394888.3:p.Arg1241=
ENST00000453981.5:c.3519C=	ENSP00000408464.2:p.Arg1173=
ENST00000469391.5:c.3423C=	ENSP00000419438.1:p.Arg1141=
ENST00000495184.5:n.5678C=
NM_001190458.1:c.3423C=	NP_001177387.1:p.Arg1141=
NM_001193536.1:c.3519C=	NP_001180465.1:p.Arg1173=
NM_203447.3:c.3723C= , LRG_196t1:c.3723C=	NP_982272.2:p.Arg1241=
XM_011518045.1:c.3423C=	XP_011516347.1:p.Arg1141=
XM_011518046.1:c.3585C=	XP_011516348.1:p.Arg1195=
XM_011518047.1:c.3519C=	XP_011516349.1:p.Arg1173=
XM_011518048.1:c.3519C=	XP_011516350.1:p.Arg1173=
XM_011518049.1:c.1959C=	XP_011516351.1:p.Arg653=
XM_011518045.3:c.3423C=	XP_011516347.1:p.Arg1141=
XM_011518046.2:c.3585C=	XP_011516348.1:p.Arg1195=
XM_011518047.3:c.3519C=	XP_011516349.1:p.Arg1173=
XM_011518048.2:c.3519C=	XP_011516350.1:p.Arg1173=
XM_011518049.2:c.1959C=	XP_011516351.1:p.Arg653=
XM_017015173.1:c.3519C=	XP_016870662.1:p.Arg1173=
XM_017015174.1:c.3585C=	XP_016870663.1:p.Arg1195=
NM_001190458.2:c.3423C=	NP_001177387.1:p.Arg1141=
NM_001193536.2:c.3519C=	NP_001180465.1:p.Arg1173=
NM_203447.4:c.3723C= MANE Select	NP_982272.2:p.Arg1241=