Canonical Allele Identifier: CA372769722

Gene: DOCK8

Linked Data

• MyVariant Identifiers: chr9:g.452057A>G (hg19) ; chr9:g.452057A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.452057A>G , CM000671.2:g.452057A>G	GRCh38
NC_000009.11:g.452057A>G , CM000671.1:g.452057A>G	GRCh37
NC_000009.10:g.442057A>G	NCBI36
NG_017007.1:g.242193A>G , LRG_196:g.242193A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382329.2:c.5708A>G	ENSP00000371766.2:p.Asp1903Gly
ENST00000683406.1:n.2483A>G
ENST00000684637.1:n.1689A>G
ENST00000685949.1:n.4796A>G
ENST00000432829.7:c.6008A>G MANE Select	ENSP00000394888.3:p.Asp2003Gly
ENST00000382329.1:c.4409A>G	ENSP00000371766.1:p.Asp1470Gly
ENST00000432829.6:c.6008A>G	ENSP00000394888.3:p.Asp2003Gly
ENST00000453981.5:c.5804A>G	ENSP00000408464.2:p.Asp1935Gly
ENST00000469391.5:c.5708A>G	ENSP00000419438.1:p.Asp1903Gly
ENST00000495184.5:n.7963A>G
NM_001190458.1:c.5708A>G	NP_001177387.1:p.Asp1903Gly
NM_001193536.1:c.5804A>G	NP_001180465.1:p.Asp1935Gly
NM_203447.3:c.6008A>G , LRG_196t1:c.6008A>G	NP_982272.2:p.Asp2003Gly
XM_011518045.1:c.5708A>G	XP_011516347.1:p.Asp1903Gly
XM_011518046.1:c.5870A>G	XP_011516348.1:p.Asp1957Gly
XM_011518047.1:c.5804A>G	XP_011516349.1:p.Asp1935Gly
XM_011518048.1:c.5804A>G	XP_011516350.1:p.Asp1935Gly
XM_011518049.1:c.4244A>G	XP_011516351.1:p.Asp1415Gly
XM_011518045.3:c.5708A>G	XP_011516347.1:p.Asp1903Gly
XM_011518046.2:c.5870A>G	XP_011516348.1:p.Asp1957Gly
XM_011518047.3:c.5804A>G	XP_011516349.1:p.Asp1935Gly
XM_011518048.2:c.5804A>G	XP_011516350.1:p.Asp1935Gly
XM_011518049.2:c.4244A>G	XP_011516351.1:p.Asp1415Gly
XM_017015173.1:c.5804A>G	XP_016870662.1:p.Asp1935Gly
XM_017015174.1:c.5870A>G	XP_016870663.1:p.Asp1957Gly
NM_001190458.2:c.5708A>G	NP_001177387.1:p.Asp1903Gly
NM_001193536.2:c.5804A>G	NP_001180465.1:p.Asp1935Gly
NM_203447.4:c.6008A>G MANE Select	NP_982272.2:p.Asp2003Gly