Canonical Allele Identifier: CA1826807594

Gene: DOCK8

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.271629A= , CM000671.2:g.271629A=	GRCh38
NC_000009.11:g.271629A= , CM000671.1:g.271629A=	GRCh37
NC_000009.10:g.261629A=	NCBI36
NG_017007.1:g.61765A= , LRG_196:g.61765A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000382329.2:c.-149A=	ENSP00000371766.2:n.-149A=
ENST00000682121.1:n.166-14832A=
ENST00000684166.1:n.165A=
ENST00000684384.1:n.165A=
ENST00000432829.7:c.56A= MANE Select	ENSP00000394888.3:p.Tyr19=
ENST00000432829.6:c.56A=	ENSP00000394888.3:p.Tyr19=
ENST00000454469.6:n.165A=
ENST00000469197.5:c.56A=	ENSP00000418587.1:p.Tyr19=
ENST00000479404.5:c.-149A=	ENSP00000417082.1:n.-149A=
ENST00000524396.5:c.*19A=	ENSP00000436628.1:n.*19A=
NM_203447.3:c.56A= , LRG_196t1:c.56A=	NP_982272.2:p.Tyr19=
XM_011518045.1:c.-149A=	XP_011516347.1:n.-149A=
XM_011518047.1:c.-149A=	XP_011516349.1:n.-149A=
XR_929404.1:n.88+1276T=
XR_929406.1:n.1333+2655T=
XM_011518045.3:c.-149A=	XP_011516347.1:n.-149A=
XM_011518047.3:c.-149A=	XP_011516349.1:n.-149A=
XM_017015173.1:c.-149A=	XP_016870662.1:n.-149A=
NM_203447.4:c.56A= MANE Select	NP_982272.2:p.Tyr19=