Canonical Allele Identifier: CA463848574

Gene: DOCK8

Linked Data

• ClinVar Variation Id: 2787480
• ClinVar RCV Id: RCV003762271
• gnomAD v4: 9-377159-G-T
• MyVariant Identifiers: chr9:g.377159G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.377159G>T , CM000671.2:g.377159G>T	GRCh38
NC_000009.11:g.377159G>T , CM000671.1:g.377159G>T	GRCh37
NC_000009.10:g.367159G>T	NCBI36
NG_017007.1:g.167295G>T , LRG_196:g.167295G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382329.2:c.2184G>T	ENSP00000371766.2:p.Leu728=
ENST00000382331.6:n.885G>T
ENST00000483757.6:c.*1075G>T	ENSP00000417691.2:n.*1075G>T
ENST00000682260.1:n.2284G>T
ENST00000685949.1:n.1176G>T
ENST00000432829.7:c.2388G>T MANE Select	ENSP00000394888.3:p.Leu796=
ENST00000382329.1:c.789G>T	ENSP00000371766.1:p.Leu263=
ENST00000382331.5:c.294G>T	ENSP00000371768.1:p.Leu98=
ENST00000432829.6:c.2388G>T	ENSP00000394888.3:p.Leu796=
ENST00000453981.5:c.2184G>T	ENSP00000408464.2:p.Leu728=
ENST00000469391.5:c.2184G>T	ENSP00000419438.1:p.Leu728=
ENST00000483757.5:c.*1863G>T	ENSP00000417691.1:n.*1863G>T
ENST00000495184.5:n.4343G>T
NM_001190458.1:c.2184G>T	NP_001177387.1:p.Leu728=
NM_001193536.1:c.2184G>T	NP_001180465.1:p.Leu728=
NM_203447.3:c.2388G>T , LRG_196t1:c.2388G>T	NP_982272.2:p.Leu796=
XM_011518045.1:c.2184G>T	XP_011516347.1:p.Leu728=
XM_011518046.1:c.2250G>T	XP_011516348.1:p.Leu750=
XM_011518047.1:c.2184G>T	XP_011516349.1:p.Leu728=
XM_011518048.1:c.2184G>T	XP_011516350.1:p.Leu728=
XM_011518049.1:c.624G>T	XP_011516351.1:p.Leu208=
XM_011518045.3:c.2184G>T	XP_011516347.1:p.Leu728=
XM_011518046.2:c.2250G>T	XP_011516348.1:p.Leu750=
XM_011518047.3:c.2184G>T	XP_011516349.1:p.Leu728=
XM_011518048.2:c.2184G>T	XP_011516350.1:p.Leu728=
XM_011518049.2:c.624G>T	XP_011516351.1:p.Leu208=
XM_017015173.1:c.2184G>T	XP_016870662.1:p.Leu728=
XM_017015174.1:c.2250G>T	XP_016870663.1:p.Leu750=
NM_001190458.2:c.2184G>T	NP_001177387.1:p.Leu728=
NM_001193536.2:c.2184G>T	NP_001180465.1:p.Leu728=
NM_203447.4:c.2388G>T MANE Select	NP_982272.2:p.Leu796=