Canonical Allele Identifier: CA372760530

Gene: DOCK8

Linked Data

• dbSNP Id: rs139391329
• MyVariant Identifiers: chr9:g.312088C>G (hg19) ; chr9:g.312088C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.312088C>G , CM000671.2:g.312088C>G	GRCh38
NC_000009.11:g.312088C>G , CM000671.1:g.312088C>G	GRCh37
NC_000009.10:g.302088C>G	NCBI36
NG_017007.1:g.102224C>G , LRG_196:g.102224C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382329.2:c.459C>G	ENSP00000371766.2:p.Asp153Glu
ENST00000474772.2:n.109C>G
ENST00000483757.6:c.459C>G	ENSP00000417691.2:p.Asp153Glu
ENST00000682249.1:c.459C>G	ENSP00000507731.1:p.Asp153Glu
ENST00000684384.1:n.772C>G
ENST00000432829.7:c.663C>G MANE Select	ENSP00000394888.3:p.Asp221Glu
ENST00000382341.5:n.558C>G
ENST00000432829.6:c.663C>G	ENSP00000394888.3:p.Asp221Glu
ENST00000453981.5:c.459C>G	ENSP00000408464.2:p.Asp153Glu
ENST00000454469.6:n.772C>G
ENST00000469391.5:c.459C>G	ENSP00000419438.1:p.Asp153Glu
ENST00000474772.1:n.131C>G
ENST00000478380.5:n.542C>G
ENST00000483757.5:c.459C>G	ENSP00000417691.1:p.Asp153Glu
ENST00000495184.5:n.524C>G
ENST00000524396.5:c.*626C>G	ENSP00000436628.1:n.*626C>G
NM_001190458.1:c.459C>G	NP_001177387.1:p.Asp153Glu
NM_001193536.1:c.459C>G	NP_001180465.1:p.Asp153Glu
NM_203447.3:c.663C>G , LRG_196t1:c.663C>G	NP_982272.2:p.Asp221Glu
XM_011518045.1:c.459C>G	XP_011516347.1:p.Asp153Glu
XM_011518046.1:c.525C>G	XP_011516348.1:p.Asp175Glu
XM_011518047.1:c.459C>G	XP_011516349.1:p.Asp153Glu
XM_011518048.1:c.459C>G	XP_011516350.1:p.Asp153Glu
XM_011518045.3:c.459C>G	XP_011516347.1:p.Asp153Glu
XM_011518046.2:c.525C>G	XP_011516348.1:p.Asp175Glu
XM_011518047.3:c.459C>G	XP_011516349.1:p.Asp153Glu
XM_011518048.2:c.459C>G	XP_011516350.1:p.Asp153Glu
XM_017015173.1:c.459C>G	XP_016870662.1:p.Asp153Glu
XM_017015174.1:c.525C>G	XP_016870663.1:p.Asp175Glu
NM_001190458.2:c.459C>G	NP_001177387.1:p.Asp153Glu
NM_001193536.2:c.459C>G	NP_001180465.1:p.Asp153Glu
NM_203447.4:c.663C>G MANE Select	NP_982272.2:p.Asp221Glu