Canonical Allele Identifier: CA372763261

Gene: DOCK8

Linked Data

• MyVariant Identifiers: chr9:g.377091A>G (hg19) ; chr9:g.377091A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.377091A>G , CM000671.2:g.377091A>G	GRCh38
NC_000009.11:g.377091A>G , CM000671.1:g.377091A>G	GRCh37
NC_000009.10:g.367091A>G	NCBI36
NG_017007.1:g.167227A>G , LRG_196:g.167227A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382329.2:c.2116A>G	ENSP00000371766.2:p.Lys706Glu
ENST00000382331.6:n.817A>G
ENST00000483757.6:c.*1007A>G	ENSP00000417691.2:n.*1007A>G
ENST00000682260.1:n.2216A>G
ENST00000685949.1:n.1108A>G
ENST00000432829.7:c.2320A>G MANE Select	ENSP00000394888.3:p.Lys774Glu
ENST00000382329.1:c.721A>G	ENSP00000371766.1:p.Lys241Glu
ENST00000382331.5:c.226A>G	ENSP00000371768.1:p.Lys76Glu
ENST00000432829.6:c.2320A>G	ENSP00000394888.3:p.Lys774Glu
ENST00000453981.5:c.2116A>G	ENSP00000408464.2:p.Lys706Glu
ENST00000469391.5:c.2116A>G	ENSP00000419438.1:p.Lys706Glu
ENST00000483757.5:c.*1795A>G	ENSP00000417691.1:n.*1795A>G
ENST00000495184.5:n.4275A>G
NM_001190458.1:c.2116A>G	NP_001177387.1:p.Lys706Glu
NM_001193536.1:c.2116A>G	NP_001180465.1:p.Lys706Glu
NM_203447.3:c.2320A>G , LRG_196t1:c.2320A>G	NP_982272.2:p.Lys774Glu
XM_011518045.1:c.2116A>G	XP_011516347.1:p.Lys706Glu
XM_011518046.1:c.2182A>G	XP_011516348.1:p.Lys728Glu
XM_011518047.1:c.2116A>G	XP_011516349.1:p.Lys706Glu
XM_011518048.1:c.2116A>G	XP_011516350.1:p.Lys706Glu
XM_011518049.1:c.556A>G	XP_011516351.1:p.Lys186Glu
XM_011518045.3:c.2116A>G	XP_011516347.1:p.Lys706Glu
XM_011518046.2:c.2182A>G	XP_011516348.1:p.Lys728Glu
XM_011518047.3:c.2116A>G	XP_011516349.1:p.Lys706Glu
XM_011518048.2:c.2116A>G	XP_011516350.1:p.Lys706Glu
XM_011518049.2:c.556A>G	XP_011516351.1:p.Lys186Glu
XM_017015173.1:c.2116A>G	XP_016870662.1:p.Lys706Glu
XM_017015174.1:c.2182A>G	XP_016870663.1:p.Lys728Glu
NM_001190458.2:c.2116A>G	NP_001177387.1:p.Lys706Glu
NM_001193536.2:c.2116A>G	NP_001180465.1:p.Lys706Glu
NM_203447.4:c.2320A>G MANE Select	NP_982272.2:p.Lys774Glu