Canonical Allele Identifier: CA1826902372

Gene: DOCK8

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.441446T= , CM000671.2:g.441446T=	GRCh38
NC_000009.11:g.441446T= , CM000671.1:g.441446T=	GRCh37
NC_000009.10:g.431446T=	NCBI36
NG_017007.1:g.231582T= , LRG_196:g.231582T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382329.2:c.5055+29T=	ENSP00000371766.2:n.5055+29T=
ENST00000683406.1:n.1830+29T=
ENST00000684637.1:n.1036+29T=
ENST00000685949.1:n.4143+29T=
ENST00000432829.7:c.5355+29T= MANE Select	ENSP00000394888.3:n.5355+29T=
ENST00000382329.1:c.3756+29T=	ENSP00000371766.1:n.3756+29T=
ENST00000432829.6:c.5355+29T=	ENSP00000394888.3:n.5355+29T=
ENST00000453981.5:c.5151+29T=	ENSP00000408464.2:n.5151+29T=
ENST00000469391.5:c.5055+29T=	ENSP00000419438.1:n.5055+29T=
ENST00000495184.5:n.7310+29T=
NM_001190458.1:c.5055+29T=	NP_001177387.1:n.5055+29T=
NM_001193536.1:c.5151+29T=	NP_001180465.1:n.5151+29T=
NM_203447.3:c.5355+29T= , LRG_196t1:c.5355+29T=	NP_982272.2:n.5355+29T=
XM_011518045.1:c.5055+29T=	XP_011516347.1:n.5055+29T=
XM_011518046.1:c.5217+29T=	XP_011516348.1:n.5217+29T=
XM_011518047.1:c.5151+29T=	XP_011516349.1:n.5151+29T=
XM_011518048.1:c.5151+29T=	XP_011516350.1:n.5151+29T=
XM_011518049.1:c.3591+29T=	XP_011516351.1:n.3591+29T=
XM_011518045.3:c.5055+29T=	XP_011516347.1:n.5055+29T=
XM_011518046.2:c.5217+29T=	XP_011516348.1:n.5217+29T=
XM_011518047.3:c.5151+29T=	XP_011516349.1:n.5151+29T=
XM_011518048.2:c.5151+29T=	XP_011516350.1:n.5151+29T=
XM_011518049.2:c.3591+29T=	XP_011516351.1:n.3591+29T=
XM_017015173.1:c.5151+29T=	XP_016870662.1:n.5151+29T=
XM_017015174.1:c.5217+29T=	XP_016870663.1:n.5217+29T=
NM_001190458.2:c.5055+29T=	NP_001177387.1:n.5055+29T=
NM_001193536.2:c.5151+29T=	NP_001180465.1:n.5151+29T=
NM_203447.4:c.5355+29T= MANE Select	NP_982272.2:n.5355+29T=