Canonical Allele Identifier: CA463701270

Gene: DOCK8

Linked Data

• MyVariant Identifiers: chr9:g.452055T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.452055T>G , CM000671.2:g.452055T>G	GRCh38
NC_000009.11:g.452055T>G , CM000671.1:g.452055T>G	GRCh37
NC_000009.10:g.442055T>G	NCBI36
NG_017007.1:g.242191T>G , LRG_196:g.242191T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382329.2:c.5706T>G	ENSP00000371766.2:p.Ala1902=
ENST00000683406.1:n.2481T>G
ENST00000684637.1:n.1687T>G
ENST00000685949.1:n.4794T>G
ENST00000432829.7:c.6006T>G MANE Select	ENSP00000394888.3:p.Ala2002=
ENST00000382329.1:c.4407T>G	ENSP00000371766.1:p.Ala1469=
ENST00000432829.6:c.6006T>G	ENSP00000394888.3:p.Ala2002=
ENST00000453981.5:c.5802T>G	ENSP00000408464.2:p.Ala1934=
ENST00000469391.5:c.5706T>G	ENSP00000419438.1:p.Ala1902=
ENST00000495184.5:n.7961T>G
NM_001190458.1:c.5706T>G	NP_001177387.1:p.Ala1902=
NM_001193536.1:c.5802T>G	NP_001180465.1:p.Ala1934=
NM_203447.3:c.6006T>G , LRG_196t1:c.6006T>G	NP_982272.2:p.Ala2002=
XM_011518045.1:c.5706T>G	XP_011516347.1:p.Ala1902=
XM_011518046.1:c.5868T>G	XP_011516348.1:p.Ala1956=
XM_011518047.1:c.5802T>G	XP_011516349.1:p.Ala1934=
XM_011518048.1:c.5802T>G	XP_011516350.1:p.Ala1934=
XM_011518049.1:c.4242T>G	XP_011516351.1:p.Ala1414=
XM_011518045.3:c.5706T>G	XP_011516347.1:p.Ala1902=
XM_011518046.2:c.5868T>G	XP_011516348.1:p.Ala1956=
XM_011518047.3:c.5802T>G	XP_011516349.1:p.Ala1934=
XM_011518048.2:c.5802T>G	XP_011516350.1:p.Ala1934=
XM_011518049.2:c.4242T>G	XP_011516351.1:p.Ala1414=
XM_017015173.1:c.5802T>G	XP_016870662.1:p.Ala1934=
XM_017015174.1:c.5868T>G	XP_016870663.1:p.Ala1956=
NM_001190458.2:c.5706T>G	NP_001177387.1:p.Ala1902=
NM_001193536.2:c.5802T>G	NP_001180465.1:p.Ala1934=
NM_203447.4:c.6006T>G MANE Select	NP_982272.2:p.Ala2002=