Canonical Allele Identifier: CA463848350

Gene: DOCK8

Linked Data

• COSMIC: COSM5964971 ; COSM5964972
• MyVariant Identifiers: chr9:g.377042C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.377042C>T , CM000671.2:g.377042C>T	GRCh38
NC_000009.11:g.377042C>T , CM000671.1:g.377042C>T	GRCh37
NC_000009.10:g.367042C>T	NCBI36
NG_017007.1:g.167178C>T , LRG_196:g.167178C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382329.2:c.2067C>T	ENSP00000371766.2:p.Ile689=
ENST00000382331.6:n.768C>T
ENST00000483757.6:c.*958C>T	ENSP00000417691.2:n.*958C>T
ENST00000682260.1:n.2167C>T
ENST00000685949.1:n.1059C>T
ENST00000432829.7:c.2271C>T MANE Select	ENSP00000394888.3:p.Ile757=
ENST00000382329.1:c.672C>T	ENSP00000371766.1:p.Ile224=
ENST00000382331.5:c.177C>T	ENSP00000371768.1:p.Ile59=
ENST00000432829.6:c.2271C>T	ENSP00000394888.3:p.Ile757=
ENST00000453981.5:c.2067C>T	ENSP00000408464.2:p.Ile689=
ENST00000469391.5:c.2067C>T	ENSP00000419438.1:p.Ile689=
ENST00000483757.5:c.*1746C>T	ENSP00000417691.1:n.*1746C>T
ENST00000495184.5:n.4226C>T
NM_001190458.1:c.2067C>T	NP_001177387.1:p.Ile689=
NM_001193536.1:c.2067C>T	NP_001180465.1:p.Ile689=
NM_203447.3:c.2271C>T , LRG_196t1:c.2271C>T	NP_982272.2:p.Ile757=
XM_011518045.1:c.2067C>T	XP_011516347.1:p.Ile689=
XM_011518046.1:c.2133C>T	XP_011516348.1:p.Ile711=
XM_011518047.1:c.2067C>T	XP_011516349.1:p.Ile689=
XM_011518048.1:c.2067C>T	XP_011516350.1:p.Ile689=
XM_011518049.1:c.507C>T	XP_011516351.1:p.Ile169=
XM_011518045.3:c.2067C>T	XP_011516347.1:p.Ile689=
XM_011518046.2:c.2133C>T	XP_011516348.1:p.Ile711=
XM_011518047.3:c.2067C>T	XP_011516349.1:p.Ile689=
XM_011518048.2:c.2067C>T	XP_011516350.1:p.Ile689=
XM_011518049.2:c.507C>T	XP_011516351.1:p.Ile169=
XM_017015173.1:c.2067C>T	XP_016870662.1:p.Ile689=
XM_017015174.1:c.2133C>T	XP_016870663.1:p.Ile711=
NM_001190458.2:c.2067C>T	NP_001177387.1:p.Ile689=
NM_001193536.2:c.2067C>T	NP_001180465.1:p.Ile689=
NM_203447.4:c.2271C>T MANE Select	NP_982272.2:p.Ile757=