Canonical Allele Identifier: CA1630835285

Gene: DOCK8

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.271638C= , CM000671.2:g.271638C=	GRCh38
NC_000009.11:g.271638C= , CM000671.1:g.271638C=	GRCh37
NC_000009.10:g.261638C=	NCBI36
NG_017007.1:g.61774C= , LRG_196:g.61774C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000382329.2:c.-140C=	ENSP00000371766.2:n.-140C=
ENST00000682121.1:n.166-14823C=
ENST00000684166.1:n.174C=
ENST00000684384.1:n.174C=
ENST00000432829.7:c.65C= MANE Select	ENSP00000394888.3:p.Ala22=
ENST00000432829.6:c.65C=	ENSP00000394888.3:p.Ala22=
ENST00000454469.6:n.174C=
ENST00000469197.5:c.65C=	ENSP00000418587.1:p.Ala22=
ENST00000479404.5:c.-140C=	ENSP00000417082.1:n.-140C=
ENST00000524396.5:c.*28C=	ENSP00000436628.1:n.*28C=
NM_203447.3:c.65C= , LRG_196t1:c.65C=	NP_982272.2:p.Ala22=
XM_011518045.1:c.-140C=	XP_011516347.1:n.-140C=
XM_011518047.1:c.-140C=	XP_011516349.1:n.-140C=
XR_929404.1:n.88+1267G=
XR_929406.1:n.1333+2646G=
XM_011518045.3:c.-140C=	XP_011516347.1:n.-140C=
XM_011518047.3:c.-140C=	XP_011516349.1:n.-140C=
XM_017015173.1:c.-140C=	XP_016870662.1:n.-140C=
NM_203447.4:c.65C= MANE Select	NP_982272.2:p.Ala22=