Canonical Allele Identifier: CA4956918

Gene: DOCK8 DOCK8-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.215028A>G , CM000671.2:g.215028A>G	GRCh38
NC_000009.11:g.215028A>G , CM000671.1:g.215028A>G	GRCh37
NC_000009.10:g.205028A>G	NCBI36
NG_017007.1:g.5164A>G , LRG_196:g.5164A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682121.1:n.164A>G (DOCK8)
ENST00000684166.1:n.161A>G (DOCK8)
ENST00000684384.1:n.161A>G (DOCK8)
ENST00000432829.7:c.52A>G (DOCK8) MANE Select	ENSP00000394888.3:p.Arg18Gly
ENST00000382387.3:c.369T>C (DOCK8-AS1)	ENSP00000371824.2:p.Pro123=
ENST00000432829.6:c.52A>G (DOCK8)	ENSP00000394888.3:p.Arg18Gly
ENST00000454469.6:n.161A>G (DOCK8)
ENST00000469197.5:c.52A>G (DOCK8)	ENSP00000418587.1:p.Arg18Gly
ENST00000524396.5:c.52A>G (DOCK8)	ENSP00000436628.1:p.Ser18Gly
NM_152569.2:c.369T>C (DOCK8-AS1)	NP_689782.2:p.Pro123=
NM_203447.3:c.52A>G , LRG_196t1:c.52A>G (DOCK8)	NP_982272.2:p.Arg18Gly
XM_011518045.3:c.-152+3712A>G (DOCK8)	XP_011516347.1:n.-152+3712A>G
XM_017015173.1:c.-152+3712A>G (DOCK8)	XP_016870662.1:n.-152+3712A>G
NR_160804.1:n.723T>C (DOCK8-AS1)
NM_203447.4:c.52A>G (DOCK8) MANE Select	NP_982272.2:p.Arg18Gly