Canonical Allele Identifier: CA372760485

Gene: DOCK8

Linked Data

• MyVariant Identifiers: chr9:g.414841A>T (hg19) ; chr9:g.414841A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.414841A>T , CM000671.2:g.414841A>T	GRCh38
NC_000009.11:g.414841A>T , CM000671.1:g.414841A>T	GRCh37
NC_000009.10:g.404841A>T	NCBI36
NG_017007.1:g.204977A>T , LRG_196:g.204977A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382329.2:c.3290A>T	ENSP00000371766.2:p.Asp1097Val
ENST00000683406.1:n.111A>T
ENST00000685949.1:n.2378A>T
ENST00000432829.7:c.3590A>T MANE Select	ENSP00000394888.3:p.Asp1197Val
ENST00000382329.1:c.1991A>T	ENSP00000371766.1:p.Asp664Val
ENST00000432829.6:c.3590A>T	ENSP00000394888.3:p.Asp1197Val
ENST00000453981.5:c.3386A>T	ENSP00000408464.2:p.Asp1129Val
ENST00000469391.5:c.3290A>T	ENSP00000419438.1:p.Asp1097Val
ENST00000495184.5:n.5545A>T
NM_001190458.1:c.3290A>T	NP_001177387.1:p.Asp1097Val
NM_001193536.1:c.3386A>T	NP_001180465.1:p.Asp1129Val
NM_203447.3:c.3590A>T , LRG_196t1:c.3590A>T	NP_982272.2:p.Asp1197Val
XM_011518045.1:c.3290A>T	XP_011516347.1:p.Asp1097Val
XM_011518046.1:c.3452A>T	XP_011516348.1:p.Asp1151Val
XM_011518047.1:c.3386A>T	XP_011516349.1:p.Asp1129Val
XM_011518048.1:c.3386A>T	XP_011516350.1:p.Asp1129Val
XM_011518049.1:c.1826A>T	XP_011516351.1:p.Asp609Val
XM_011518045.3:c.3290A>T	XP_011516347.1:p.Asp1097Val
XM_011518046.2:c.3452A>T	XP_011516348.1:p.Asp1151Val
XM_011518047.3:c.3386A>T	XP_011516349.1:p.Asp1129Val
XM_011518048.2:c.3386A>T	XP_011516350.1:p.Asp1129Val
XM_011518049.2:c.1826A>T	XP_011516351.1:p.Asp609Val
XM_017015173.1:c.3386A>T	XP_016870662.1:p.Asp1129Val
XM_017015174.1:c.3452A>T	XP_016870663.1:p.Asp1151Val
NM_001190458.2:c.3290A>T	NP_001177387.1:p.Asp1097Val
NM_001193536.2:c.3386A>T	NP_001180465.1:p.Asp1129Val
NM_203447.4:c.3590A>T MANE Select	NP_982272.2:p.Asp1197Val