Canonical Allele Identifier: CA372760439

Gene: DOCK8

Linked Data

• MyVariant Identifiers: chr9:g.414834T>A (hg19) ; chr9:g.414834T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.414834T>A , CM000671.2:g.414834T>A	GRCh38
NC_000009.11:g.414834T>A , CM000671.1:g.414834T>A	GRCh37
NC_000009.10:g.404834T>A	NCBI36
NG_017007.1:g.204970T>A , LRG_196:g.204970T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382329.2:c.3283T>A	ENSP00000371766.2:p.Ser1095Thr
ENST00000683406.1:n.104T>A
ENST00000685949.1:n.2371T>A
ENST00000432829.7:c.3583T>A MANE Select	ENSP00000394888.3:p.Ser1195Thr
ENST00000382329.1:c.1984T>A	ENSP00000371766.1:p.Ser662Thr
ENST00000432829.6:c.3583T>A	ENSP00000394888.3:p.Ser1195Thr
ENST00000453981.5:c.3379T>A	ENSP00000408464.2:p.Ser1127Thr
ENST00000469391.5:c.3283T>A	ENSP00000419438.1:p.Ser1095Thr
ENST00000495184.5:n.5538T>A
NM_001190458.1:c.3283T>A	NP_001177387.1:p.Ser1095Thr
NM_001193536.1:c.3379T>A	NP_001180465.1:p.Ser1127Thr
NM_203447.3:c.3583T>A , LRG_196t1:c.3583T>A	NP_982272.2:p.Ser1195Thr
XM_011518045.1:c.3283T>A	XP_011516347.1:p.Ser1095Thr
XM_011518046.1:c.3445T>A	XP_011516348.1:p.Ser1149Thr
XM_011518047.1:c.3379T>A	XP_011516349.1:p.Ser1127Thr
XM_011518048.1:c.3379T>A	XP_011516350.1:p.Ser1127Thr
XM_011518049.1:c.1819T>A	XP_011516351.1:p.Ser607Thr
XM_011518045.3:c.3283T>A	XP_011516347.1:p.Ser1095Thr
XM_011518046.2:c.3445T>A	XP_011516348.1:p.Ser1149Thr
XM_011518047.3:c.3379T>A	XP_011516349.1:p.Ser1127Thr
XM_011518048.2:c.3379T>A	XP_011516350.1:p.Ser1127Thr
XM_011518049.2:c.1819T>A	XP_011516351.1:p.Ser607Thr
XM_017015173.1:c.3379T>A	XP_016870662.1:p.Ser1127Thr
XM_017015174.1:c.3445T>A	XP_016870663.1:p.Ser1149Thr
NM_001190458.2:c.3283T>A	NP_001177387.1:p.Ser1095Thr
NM_001193536.2:c.3379T>A	NP_001180465.1:p.Ser1127Thr
NM_203447.4:c.3583T>A MANE Select	NP_982272.2:p.Ser1195Thr