Canonical Allele Identifier: CA372760650

Gene: DOCK8

Linked Data

• MyVariant Identifiers: chr9:g.414868A>T (hg19) ; chr9:g.414868A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.414868A>T , CM000671.2:g.414868A>T	GRCh38
NC_000009.11:g.414868A>T , CM000671.1:g.414868A>T	GRCh37
NC_000009.10:g.404868A>T	NCBI36
NG_017007.1:g.205004A>T , LRG_196:g.205004A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382329.2:c.3317A>T	ENSP00000371766.2:p.Glu1106Val
ENST00000683406.1:n.138A>T
ENST00000685949.1:n.2405A>T
ENST00000432829.7:c.3617A>T MANE Select	ENSP00000394888.3:p.Glu1206Val
ENST00000382329.1:c.2018A>T	ENSP00000371766.1:p.Glu673Val
ENST00000432829.6:c.3617A>T	ENSP00000394888.3:p.Glu1206Val
ENST00000453981.5:c.3413A>T	ENSP00000408464.2:p.Glu1138Val
ENST00000469391.5:c.3317A>T	ENSP00000419438.1:p.Glu1106Val
ENST00000495184.5:n.5572A>T
NM_001190458.1:c.3317A>T	NP_001177387.1:p.Glu1106Val
NM_001193536.1:c.3413A>T	NP_001180465.1:p.Glu1138Val
NM_203447.3:c.3617A>T , LRG_196t1:c.3617A>T	NP_982272.2:p.Glu1206Val
XM_011518045.1:c.3317A>T	XP_011516347.1:p.Glu1106Val
XM_011518046.1:c.3479A>T	XP_011516348.1:p.Glu1160Val
XM_011518047.1:c.3413A>T	XP_011516349.1:p.Glu1138Val
XM_011518048.1:c.3413A>T	XP_011516350.1:p.Glu1138Val
XM_011518049.1:c.1853A>T	XP_011516351.1:p.Glu618Val
XM_011518045.3:c.3317A>T	XP_011516347.1:p.Glu1106Val
XM_011518046.2:c.3479A>T	XP_011516348.1:p.Glu1160Val
XM_011518047.3:c.3413A>T	XP_011516349.1:p.Glu1138Val
XM_011518048.2:c.3413A>T	XP_011516350.1:p.Glu1138Val
XM_011518049.2:c.1853A>T	XP_011516351.1:p.Glu618Val
XM_017015173.1:c.3413A>T	XP_016870662.1:p.Glu1138Val
XM_017015174.1:c.3479A>T	XP_016870663.1:p.Glu1160Val
NM_001190458.2:c.3317A>T	NP_001177387.1:p.Glu1106Val
NM_001193536.2:c.3413A>T	NP_001180465.1:p.Glu1138Val
NM_203447.4:c.3617A>T MANE Select	NP_982272.2:p.Glu1206Val