Canonical Allele Identifier: CA1826902237

Gene: DOCK8

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.441369_441371delinsACT , CM000671.2:g.441369_441371delinsACT	GRCh38
NC_000009.11:g.441369_441371delinsACT , CM000671.1:g.441369_441371delinsACT	GRCh37
NC_000009.10:g.431369_431371delinsACT	NCBI36
NG_017007.1:g.231505_231507delinsACT , LRG_196:g.231505_231507delinsACT

Transcript Alleles

HGVS	Amino-acid change
ENST00000382329.2:c.5007_5009delinsACT	ENSP00000371766.2:p.Thr1669=
ENST00000683406.1:n.1782_1784delinsACT
ENST00000684637.1:n.988_990delinsACT
ENST00000685949.1:n.4095_4097delinsACT
ENST00000432829.7:c.5307_5309delinsACT MANE Select	ENSP00000394888.3:p.Thr1769=
ENST00000382329.1:c.3708_3710delinsACT	ENSP00000371766.1:p.Thr1236=
ENST00000432829.6:c.5307_5309delinsACT	ENSP00000394888.3:p.Thr1769=
ENST00000453981.5:c.5103_5105delinsACT	ENSP00000408464.2:p.Thr1701=
ENST00000469391.5:c.5007_5009delinsACT	ENSP00000419438.1:p.Thr1669=
ENST00000495184.5:n.7262_7264delinsACT
NM_001190458.1:c.5007_5009delinsACT	NP_001177387.1:p.Thr1669=
NM_001193536.1:c.5103_5105delinsACT	NP_001180465.1:p.Thr1701=
NM_203447.3:c.5307_5309delinsACT , LRG_196t1:c.5307_5309delinsACT	NP_982272.2:p.Thr1769=
XM_011518045.1:c.5007_5009delinsACT	XP_011516347.1:p.Thr1669=
XM_011518046.1:c.5169_5171delinsACT	XP_011516348.1:p.Thr1723=
XM_011518047.1:c.5103_5105delinsACT	XP_011516349.1:p.Thr1701=
XM_011518048.1:c.5103_5105delinsACT	XP_011516350.1:p.Thr1701=
XM_011518049.1:c.3543_3545delinsACT	XP_011516351.1:p.Thr1181=
XM_011518045.3:c.5007_5009delinsACT	XP_011516347.1:p.Thr1669=
XM_011518046.2:c.5169_5171delinsACT	XP_011516348.1:p.Thr1723=
XM_011518047.3:c.5103_5105delinsACT	XP_011516349.1:p.Thr1701=
XM_011518048.2:c.5103_5105delinsACT	XP_011516350.1:p.Thr1701=
XM_011518049.2:c.3543_3545delinsACT	XP_011516351.1:p.Thr1181=
XM_017015173.1:c.5103_5105delinsACT	XP_016870662.1:p.Thr1701=
XM_017015174.1:c.5169_5171delinsACT	XP_016870663.1:p.Thr1723=
NM_001190458.2:c.5007_5009delinsACT	NP_001177387.1:p.Thr1669=
NM_001193536.2:c.5103_5105delinsACT	NP_001180465.1:p.Thr1701=
NM_203447.4:c.5307_5309delinsACT MANE Select	NP_982272.2:p.Thr1769=