Canonical Allele Identifier: CA372763244

Gene: DOCK8

Linked Data

• gnomAD v4: 9-377083-A-G
• MyVariant Identifiers: chr9:g.377083A>G (hg19) ; chr9:g.377083A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.377083A>G , CM000671.2:g.377083A>G	GRCh38
NC_000009.11:g.377083A>G , CM000671.1:g.377083A>G	GRCh37
NC_000009.10:g.367083A>G	NCBI36
NG_017007.1:g.167219A>G , LRG_196:g.167219A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382329.2:c.2108A>G	ENSP00000371766.2:p.His703Arg
ENST00000382331.6:n.809A>G
ENST00000483757.6:c.*999A>G	ENSP00000417691.2:n.*999A>G
ENST00000682260.1:n.2208A>G
ENST00000685949.1:n.1100A>G
ENST00000432829.7:c.2312A>G MANE Select	ENSP00000394888.3:p.His771Arg
ENST00000382329.1:c.713A>G	ENSP00000371766.1:p.His238Arg
ENST00000382331.5:c.218A>G	ENSP00000371768.1:p.His73Arg
ENST00000432829.6:c.2312A>G	ENSP00000394888.3:p.His771Arg
ENST00000453981.5:c.2108A>G	ENSP00000408464.2:p.His703Arg
ENST00000469391.5:c.2108A>G	ENSP00000419438.1:p.His703Arg
ENST00000483757.5:c.*1787A>G	ENSP00000417691.1:n.*1787A>G
ENST00000495184.5:n.4267A>G
NM_001190458.1:c.2108A>G	NP_001177387.1:p.His703Arg
NM_001193536.1:c.2108A>G	NP_001180465.1:p.His703Arg
NM_203447.3:c.2312A>G , LRG_196t1:c.2312A>G	NP_982272.2:p.His771Arg
XM_011518045.1:c.2108A>G	XP_011516347.1:p.His703Arg
XM_011518046.1:c.2174A>G	XP_011516348.1:p.His725Arg
XM_011518047.1:c.2108A>G	XP_011516349.1:p.His703Arg
XM_011518048.1:c.2108A>G	XP_011516350.1:p.His703Arg
XM_011518049.1:c.548A>G	XP_011516351.1:p.His183Arg
XM_011518045.3:c.2108A>G	XP_011516347.1:p.His703Arg
XM_011518046.2:c.2174A>G	XP_011516348.1:p.His725Arg
XM_011518047.3:c.2108A>G	XP_011516349.1:p.His703Arg
XM_011518048.2:c.2108A>G	XP_011516350.1:p.His703Arg
XM_011518049.2:c.548A>G	XP_011516351.1:p.His183Arg
XM_017015173.1:c.2108A>G	XP_016870662.1:p.His703Arg
XM_017015174.1:c.2174A>G	XP_016870663.1:p.His725Arg
NM_001190458.2:c.2108A>G	NP_001177387.1:p.His703Arg
NM_001193536.2:c.2108A>G	NP_001180465.1:p.His703Arg
NM_203447.4:c.2312A>G MANE Select	NP_982272.2:p.His771Arg