Canonical Allele Identifier: CA463699924

Gene: DOCK8

Linked Data

• MyVariant Identifiers: chr9:g.441358_441359insT (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.441358_441359insT , CM000671.2:g.441358_441359insT	GRCh38
NC_000009.11:g.441358_441359insT , CM000671.1:g.441358_441359insT	GRCh37
NC_000009.10:g.431358_431359insT	NCBI36
NG_017007.1:g.231494_231495insT , LRG_196:g.231494_231495insT

Transcript Alleles

HGVS	Amino-acid change
ENST00000382329.2:c.4996_4997insT	ENSP00000371766.2:p.Arg1666LeufsTer19
ENST00000683406.1:n.1771_1772insT
ENST00000684637.1:n.977_978insT
ENST00000685949.1:n.4084_4085insT
ENST00000432829.7:c.5296_5297insT MANE Select	ENSP00000394888.3:p.Arg1766LeufsTer19
ENST00000382329.1:c.3697_3698insT	ENSP00000371766.1:p.Arg1233LeufsTer19
ENST00000432829.6:c.5296_5297insT	ENSP00000394888.3:p.Arg1766LeufsTer19
ENST00000453981.5:c.5092_5093insT	ENSP00000408464.2:p.Arg1698LeufsTer19
ENST00000469391.5:c.4996_4997insT	ENSP00000419438.1:p.Arg1666LeufsTer19
ENST00000495184.5:n.7251_7252insT
NM_001190458.1:c.4996_4997insT	NP_001177387.1:p.Arg1666LeufsTer19
NM_001193536.1:c.5092_5093insT	NP_001180465.1:p.Arg1698LeufsTer19
NM_203447.3:c.5296_5297insT , LRG_196t1:c.5296_5297insT	NP_982272.2:p.Arg1766LeufsTer19
XM_011518045.1:c.4996_4997insT	XP_011516347.1:p.Arg1666LeufsTer19
XM_011518046.1:c.5158_5159insT	XP_011516348.1:p.Arg1720LeufsTer19
XM_011518047.1:c.5092_5093insT	XP_011516349.1:p.Arg1698LeufsTer19
XM_011518048.1:c.5092_5093insT	XP_011516350.1:p.Arg1698LeufsTer19
XM_011518049.1:c.3532_3533insT	XP_011516351.1:p.Arg1178LeufsTer19
XM_011518045.3:c.4996_4997insT	XP_011516347.1:p.Arg1666LeufsTer19
XM_011518046.2:c.5158_5159insT	XP_011516348.1:p.Arg1720LeufsTer19
XM_011518047.3:c.5092_5093insT	XP_011516349.1:p.Arg1698LeufsTer19
XM_011518048.2:c.5092_5093insT	XP_011516350.1:p.Arg1698LeufsTer19
XM_011518049.2:c.3532_3533insT	XP_011516351.1:p.Arg1178LeufsTer19
XM_017015173.1:c.5092_5093insT	XP_016870662.1:p.Arg1698LeufsTer19
XM_017015174.1:c.5158_5159insT	XP_016870663.1:p.Arg1720LeufsTer19
NM_001190458.2:c.4996_4997insT	NP_001177387.1:p.Arg1666LeufsTer19
NM_001193536.2:c.5092_5093insT	NP_001180465.1:p.Arg1698LeufsTer19
NM_203447.4:c.5296_5297insT MANE Select	NP_982272.2:p.Arg1766LeufsTer19