Canonical Allele Identifier: CA2549656157

Gene: DOCK8

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.331329_331426del , CM000671.2:g.331329_331426del	GRCh38
NC_000009.11:g.331329_331426del , CM000671.1:g.331329_331426del	GRCh37
NC_000009.10:g.321329_321426del	NCBI36
NG_017007.1:g.121465_121562del , LRG_196:g.121465_121562del

Transcript Alleles

HGVS	Amino-acid change
ENST00000382329.2:c.841-1069_841-972del	ENSP00000371766.2:n.841-1069_841-972del
ENST00000483757.6:c.841-1069_841-972del	ENSP00000417691.2:n.841-1069_841-972del
ENST00000432829.7:c.1045-1069_1045-972del MANE Select	ENSP00000394888.3:n.1045-1069_1045-972del...
ENST00000382341.5:n.940-1069_940-972del
ENST00000432829.6:c.1045-1069_1045-972del	ENSP00000394888.3:n.1045-1069_1045-972del...
ENST00000453981.5:c.841-1069_841-972del	ENSP00000408464.2:n.841-1069_841-972del
ENST00000454469.6:n.1154-1069_1154-972del
ENST00000469391.5:c.841-1069_841-972del	ENSP00000419438.1:n.841-1069_841-972del
ENST00000483757.5:c.841-1069_841-972del	ENSP00000417691.1:n.841-1069_841-972del
ENST00000495184.5:n.906-1069_906-972del
ENST00000524396.5:c.*1008-1069_*1008-972del	ENSP00000436628.1:n.*1008-1069_*1008-972d...
NM_001190458.1:c.841-1069_841-972del	NP_001177387.1:n.841-1069_841-972del
NM_001193536.1:c.841-1069_841-972del	NP_001180465.1:n.841-1069_841-972del
NM_203447.3:c.1045-1069_1045-972del , LRG_196t1:c.1045-1069_1045-972del	NP_982272.2:n.1045-1069_1045-972del
XM_011518045.1:c.841-1069_841-972del	XP_011516347.1:n.841-1069_841-972del
XM_011518046.1:c.907-1069_907-972del	XP_011516348.1:n.907-1069_907-972del
XM_011518047.1:c.841-1069_841-972del	XP_011516349.1:n.841-1069_841-972del
XM_011518048.1:c.841-1069_841-972del	XP_011516350.1:n.841-1069_841-972del
XM_011518045.3:c.841-1069_841-972del	XP_011516347.1:n.841-1069_841-972del
XM_011518046.2:c.907-1069_907-972del	XP_011516348.1:n.907-1069_907-972del
XM_011518047.3:c.841-1069_841-972del	XP_011516349.1:n.841-1069_841-972del
XM_011518048.2:c.841-1069_841-972del	XP_011516350.1:n.841-1069_841-972del
XM_017015173.1:c.841-1069_841-972del	XP_016870662.1:n.841-1069_841-972del
XM_017015174.1:c.907-1069_907-972del	XP_016870663.1:n.907-1069_907-972del
NM_001190458.2:c.841-1069_841-972del	NP_001177387.1:n.841-1069_841-972del
NM_001193536.2:c.841-1069_841-972del	NP_001180465.1:n.841-1069_841-972del
NM_203447.4:c.1045-1069_1045-972del MANE Select	NP_982272.2:n.1045-1069_1045-972del