Canonical Allele Identifier: CA463848304

Gene: DOCK8

Linked Data

• COSMIC: COSM5411084 ; COSM5411085
• MyVariant Identifiers: chr9:g.377003C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.377003C>T , CM000671.2:g.377003C>T	GRCh38
NC_000009.11:g.377003C>T , CM000671.1:g.377003C>T	GRCh37
NC_000009.10:g.367003C>T	NCBI36
NG_017007.1:g.167139C>T , LRG_196:g.167139C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382329.2:c.2028C>T	ENSP00000371766.2:p.Thr676=
ENST00000382331.6:n.729C>T
ENST00000483757.6:c.*919C>T	ENSP00000417691.2:n.*919C>T
ENST00000682260.1:n.2128C>T
ENST00000685949.1:n.1020C>T
ENST00000432829.7:c.2232C>T MANE Select	ENSP00000394888.3:p.Thr744=
ENST00000382329.1:c.633C>T	ENSP00000371766.1:p.Thr211=
ENST00000382331.5:c.138C>T	ENSP00000371768.1:p.Thr46=
ENST00000432829.6:c.2232C>T	ENSP00000394888.3:p.Thr744=
ENST00000453981.5:c.2028C>T	ENSP00000408464.2:p.Thr676=
ENST00000469391.5:c.2028C>T	ENSP00000419438.1:p.Thr676=
ENST00000483757.5:c.*1707C>T	ENSP00000417691.1:n.*1707C>T
ENST00000495184.5:n.4187C>T
NM_001190458.1:c.2028C>T	NP_001177387.1:p.Thr676=
NM_001193536.1:c.2028C>T	NP_001180465.1:p.Thr676=
NM_203447.3:c.2232C>T , LRG_196t1:c.2232C>T	NP_982272.2:p.Thr744=
XM_011518045.1:c.2028C>T	XP_011516347.1:p.Thr676=
XM_011518046.1:c.2094C>T	XP_011516348.1:p.Thr698=
XM_011518047.1:c.2028C>T	XP_011516349.1:p.Thr676=
XM_011518048.1:c.2028C>T	XP_011516350.1:p.Thr676=
XM_011518049.1:c.468C>T	XP_011516351.1:p.Thr156=
XM_011518045.3:c.2028C>T	XP_011516347.1:p.Thr676=
XM_011518046.2:c.2094C>T	XP_011516348.1:p.Thr698=
XM_011518047.3:c.2028C>T	XP_011516349.1:p.Thr676=
XM_011518048.2:c.2028C>T	XP_011516350.1:p.Thr676=
XM_011518049.2:c.468C>T	XP_011516351.1:p.Thr156=
XM_017015173.1:c.2028C>T	XP_016870662.1:p.Thr676=
XM_017015174.1:c.2094C>T	XP_016870663.1:p.Thr698=
NM_001190458.2:c.2028C>T	NP_001177387.1:p.Thr676=
NM_001193536.2:c.2028C>T	NP_001180465.1:p.Thr676=
NM_203447.4:c.2232C>T MANE Select	NP_982272.2:p.Thr744=