Canonical Allele Identifier: CA1826910497

Gene: DOCK8

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.451969_451991delinsATATATATATTTTTTTTTTTTTT , CM000671.2:g.451969_451991delinsATATATATATTTTTTTTTTTTTT	GRCh38
NC_000009.11:g.451969_451991delinsATATATATATTTTTTTTTTTTTT , CM000671.1:g.451969_451991delinsATATATATATTTTTTTTTTTTTT	GRCh37
NC_000009.10:g.441969_441991delinsATATATATATTTTTTTTTTTTTT	NCBI36
NG_017007.1:g.242105_242127delinsATATATATATTTTTTTTTTTTTT , LRG_196:g.242105_242127delinsATATATATATTTTTTTTTTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382329.2:c.5662-42_5662-20delinsATATATATATTTTTTTTTTTTTT	ENSP00000371766.2:n.5662-42_5662-20delinsATATATATATTTTTTTTTTT...
ENST00000683406.1:n.2437-42_2437-20delinsATATATATATTTTTTTTTTTTTT
ENST00000684637.1:n.1643-42_1643-20delinsATATATATATTTTTTTTTTTTTT
ENST00000685949.1:n.4750-42_4750-20delinsATATATATATTTTTTTTTTTTTT
ENST00000432829.7:c.5962-42_5962-20delinsATATATATATTTTTTTTTTTTTT MANE Select	ENSP00000394888.3:n.5962-42_5962-20delinsATATATATATTTTTTTTTTT...
ENST00000382329.1:c.4363-42_4363-20delinsATATATATATTTTTTTTTTTTTT	ENSP00000371766.1:n.4363-42_4363-20delinsATATATATATTTTTTTTTTT...
ENST00000432829.6:c.5962-42_5962-20delinsATATATATATTTTTTTTTTTTTT	ENSP00000394888.3:n.5962-42_5962-20delinsATATATATATTTTTTTTTTT...
ENST00000453981.5:c.5758-42_5758-20delinsATATATATATTTTTTTTTTTTTT	ENSP00000408464.2:n.5758-42_5758-20delinsATATATATATTTTTTTTTTT...
ENST00000469391.5:c.5662-42_5662-20delinsATATATATATTTTTTTTTTTTTT	ENSP00000419438.1:n.5662-42_5662-20delinsATATATATATTTTTTTTTTT...
ENST00000495184.5:n.7917-42_7917-20delinsATATATATATTTTTTTTTTTTTT
NM_001190458.1:c.5662-42_5662-20delinsATATATATATTTTTTTTTTTTTT	NP_001177387.1:n.5662-42_5662-20delinsATATATATATTTTTTTTTTTTTT...
NM_001193536.1:c.5758-42_5758-20delinsATATATATATTTTTTTTTTTTTT	NP_001180465.1:n.5758-42_5758-20delinsATATATATATTTTTTTTTTTTTT...
NM_203447.3:c.5962-42_5962-20delinsATATATATATTTTTTTTTTTTTT , LRG_196t1:c.5962-42_5962-20delinsATATATATATTTTTTTTTTTTTT	NP_982272.2:n.5962-42_5962-20delinsATATATATATTTTTTTTTTTTTT
XM_011518045.1:c.5662-42_5662-20delinsATATATATATTTTTTTTTTTTTT	XP_011516347.1:n.5662-42_5662-20delinsATATATATATTTTTTTTTTTTTT...
XM_011518046.1:c.5824-42_5824-20delinsATATATATATTTTTTTTTTTTTT	XP_011516348.1:n.5824-42_5824-20delinsATATATATATTTTTTTTTTTTTT...
XM_011518047.1:c.5758-42_5758-20delinsATATATATATTTTTTTTTTTTTT	XP_011516349.1:n.5758-42_5758-20delinsATATATATATTTTTTTTTTTTTT...
XM_011518048.1:c.5758-42_5758-20delinsATATATATATTTTTTTTTTTTTT	XP_011516350.1:n.5758-42_5758-20delinsATATATATATTTTTTTTTTTTTT...
XM_011518049.1:c.4198-42_4198-20delinsATATATATATTTTTTTTTTTTTT	XP_011516351.1:n.4198-42_4198-20delinsATATATATATTTTTTTTTTTTTT...
XM_011518045.3:c.5662-42_5662-20delinsATATATATATTTTTTTTTTTTTT	XP_011516347.1:n.5662-42_5662-20delinsATATATATATTTTTTTTTTTTTT...
XM_011518046.2:c.5824-42_5824-20delinsATATATATATTTTTTTTTTTTTT	XP_011516348.1:n.5824-42_5824-20delinsATATATATATTTTTTTTTTTTTT...
XM_011518047.3:c.5758-42_5758-20delinsATATATATATTTTTTTTTTTTTT	XP_011516349.1:n.5758-42_5758-20delinsATATATATATTTTTTTTTTTTTT...
XM_011518048.2:c.5758-42_5758-20delinsATATATATATTTTTTTTTTTTTT	XP_011516350.1:n.5758-42_5758-20delinsATATATATATTTTTTTTTTTTTT...
XM_011518049.2:c.4198-42_4198-20delinsATATATATATTTTTTTTTTTTTT	XP_011516351.1:n.4198-42_4198-20delinsATATATATATTTTTTTTTTTTTT...
XM_017015173.1:c.5758-42_5758-20delinsATATATATATTTTTTTTTTTTTT	XP_016870662.1:n.5758-42_5758-20delinsATATATATATTTTTTTTTTTTTT...
XM_017015174.1:c.5824-42_5824-20delinsATATATATATTTTTTTTTTTTTT	XP_016870663.1:n.5824-42_5824-20delinsATATATATATTTTTTTTTTTTTT...
NM_001190458.2:c.5662-42_5662-20delinsATATATATATTTTTTTTTTTTTT	NP_001177387.1:n.5662-42_5662-20delinsATATATATATTTTTTTTTTTTTT...
NM_001193536.2:c.5758-42_5758-20delinsATATATATATTTTTTTTTTTTTT	NP_001180465.1:n.5758-42_5758-20delinsATATATATATTTTTTTTTTTTTT...
NM_203447.4:c.5962-42_5962-20delinsATATATATATTTTTTTTTTTTTT MANE Select	NP_982272.2:n.5962-42_5962-20delinsATATATATATTTTTTTTTTTTTT