Canonical Allele Identifier: CA1826910256

Gene: DOCK8

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.451749_451753delinsTTTTG , CM000671.2:g.451749_451753delinsTTTTG	GRCh38
NC_000009.11:g.451749_451753delinsTTTTG , CM000671.1:g.451749_451753delinsTTTTG	GRCh37
NC_000009.10:g.441749_441753delinsTTTTG	NCBI36
NG_017007.1:g.241885_241889delinsTTTTG , LRG_196:g.241885_241889delinsTTTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382329.2:c.5662-262_5662-258delinsTTTTG	ENSP00000371766.2:n.5662-262_5662-258delinsTTTTG
ENST00000683406.1:n.2437-262_2437-258delinsTTTTG
ENST00000684637.1:n.1643-262_1643-258delinsTTTTG
ENST00000685949.1:n.4750-262_4750-258delinsTTTTG
ENST00000432829.7:c.5962-262_5962-258delinsTTTTG MANE Select	ENSP00000394888.3:n.5962-262_5962-258delinsTTTTG
ENST00000382329.1:c.4363-262_4363-258delinsTTTTG	ENSP00000371766.1:n.4363-262_4363-258delinsTTTTG
ENST00000432829.6:c.5962-262_5962-258delinsTTTTG	ENSP00000394888.3:n.5962-262_5962-258delinsTTTTG
ENST00000453981.5:c.5758-262_5758-258delinsTTTTG	ENSP00000408464.2:n.5758-262_5758-258delinsTTTTG
ENST00000469391.5:c.5662-262_5662-258delinsTTTTG	ENSP00000419438.1:n.5662-262_5662-258delinsTTTTG
ENST00000495184.5:n.7917-262_7917-258delinsTTTTG
NM_001190458.1:c.5662-262_5662-258delinsTTTTG	NP_001177387.1:n.5662-262_5662-258delinsTTTTG
NM_001193536.1:c.5758-262_5758-258delinsTTTTG	NP_001180465.1:n.5758-262_5758-258delinsTTTTG
NM_203447.3:c.5962-262_5962-258delinsTTTTG , LRG_196t1:c.5962-262_5962-258delinsTTTTG	NP_982272.2:n.5962-262_5962-258delinsTTTTG
XM_011518045.1:c.5662-262_5662-258delinsTTTTG	XP_011516347.1:n.5662-262_5662-258delinsTTTTG
XM_011518046.1:c.5824-262_5824-258delinsTTTTG	XP_011516348.1:n.5824-262_5824-258delinsTTTTG
XM_011518047.1:c.5758-262_5758-258delinsTTTTG	XP_011516349.1:n.5758-262_5758-258delinsTTTTG
XM_011518048.1:c.5758-262_5758-258delinsTTTTG	XP_011516350.1:n.5758-262_5758-258delinsTTTTG
XM_011518049.1:c.4198-262_4198-258delinsTTTTG	XP_011516351.1:n.4198-262_4198-258delinsTTTTG
XM_011518045.3:c.5662-262_5662-258delinsTTTTG	XP_011516347.1:n.5662-262_5662-258delinsTTTTG
XM_011518046.2:c.5824-262_5824-258delinsTTTTG	XP_011516348.1:n.5824-262_5824-258delinsTTTTG
XM_011518047.3:c.5758-262_5758-258delinsTTTTG	XP_011516349.1:n.5758-262_5758-258delinsTTTTG
XM_011518048.2:c.5758-262_5758-258delinsTTTTG	XP_011516350.1:n.5758-262_5758-258delinsTTTTG
XM_011518049.2:c.4198-262_4198-258delinsTTTTG	XP_011516351.1:n.4198-262_4198-258delinsTTTTG
XM_017015173.1:c.5758-262_5758-258delinsTTTTG	XP_016870662.1:n.5758-262_5758-258delinsTTTTG
XM_017015174.1:c.5824-262_5824-258delinsTTTTG	XP_016870663.1:n.5824-262_5824-258delinsTTTTG
NM_001190458.2:c.5662-262_5662-258delinsTTTTG	NP_001177387.1:n.5662-262_5662-258delinsTTTTG
NM_001193536.2:c.5758-262_5758-258delinsTTTTG	NP_001180465.1:n.5758-262_5758-258delinsTTTTG
NM_203447.4:c.5962-262_5962-258delinsTTTTG MANE Select	NP_982272.2:n.5962-262_5962-258delinsTTTTG