Canonical Allele Identifier: CA463848576

Gene: DOCK8

Linked Data

• gnomAD v4: 9-377165-G-A
• MyVariant Identifiers: chr9:g.377165G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.377165G>A , CM000671.2:g.377165G>A	GRCh38
NC_000009.11:g.377165G>A , CM000671.1:g.377165G>A	GRCh37
NC_000009.10:g.367165G>A	NCBI36
NG_017007.1:g.167301G>A , LRG_196:g.167301G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382329.2:c.2190G>A	ENSP00000371766.2:p.Lys730=
ENST00000382331.6:n.891G>A
ENST00000483757.6:c.*1081G>A	ENSP00000417691.2:n.*1081G>A
ENST00000682260.1:n.2290G>A
ENST00000685949.1:n.1182G>A
ENST00000432829.7:c.2394G>A MANE Select	ENSP00000394888.3:p.Lys798=
ENST00000382329.1:c.795G>A	ENSP00000371766.1:p.Lys265=
ENST00000382331.5:c.300G>A	ENSP00000371768.1:p.Lys100=
ENST00000432829.6:c.2394G>A	ENSP00000394888.3:p.Lys798=
ENST00000453981.5:c.2190G>A	ENSP00000408464.2:p.Lys730=
ENST00000469391.5:c.2190G>A	ENSP00000419438.1:p.Lys730=
ENST00000483757.5:c.*1869G>A	ENSP00000417691.1:n.*1869G>A
ENST00000495184.5:n.4349G>A
NM_001190458.1:c.2190G>A	NP_001177387.1:p.Lys730=
NM_001193536.1:c.2190G>A	NP_001180465.1:p.Lys730=
NM_203447.3:c.2394G>A , LRG_196t1:c.2394G>A	NP_982272.2:p.Lys798=
XM_011518045.1:c.2190G>A	XP_011516347.1:p.Lys730=
XM_011518046.1:c.2256G>A	XP_011516348.1:p.Lys752=
XM_011518047.1:c.2190G>A	XP_011516349.1:p.Lys730=
XM_011518048.1:c.2190G>A	XP_011516350.1:p.Lys730=
XM_011518049.1:c.630G>A	XP_011516351.1:p.Lys210=
XM_011518045.3:c.2190G>A	XP_011516347.1:p.Lys730=
XM_011518046.2:c.2256G>A	XP_011516348.1:p.Lys752=
XM_011518047.3:c.2190G>A	XP_011516349.1:p.Lys730=
XM_011518048.2:c.2190G>A	XP_011516350.1:p.Lys730=
XM_011518049.2:c.630G>A	XP_011516351.1:p.Lys210=
XM_017015173.1:c.2190G>A	XP_016870662.1:p.Lys730=
XM_017015174.1:c.2256G>A	XP_016870663.1:p.Lys752=
NM_001190458.2:c.2190G>A	NP_001177387.1:p.Lys730=
NM_001193536.2:c.2190G>A	NP_001180465.1:p.Lys730=
NM_203447.4:c.2394G>A MANE Select	NP_982272.2:p.Lys798=