Canonical Allele Identifier: CA864780457

Gene: DOCK8

Linked Data

• dbSNP Id: rs1349003261
• MyVariant Identifiers: chr9:g.451938_451939insATGC (hg19) ; chr9:g.451938_451939insATGC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.451940_451941insGCAT , CM000671.2:g.451940_451941insGCAT	GRCh38
NC_000009.11:g.451940_451941insGCAT , CM000671.1:g.451940_451941insGCAT	GRCh37
NC_000009.10:g.441940_441941insGCAT	NCBI36
NG_017007.1:g.242076_242077insGCAT , LRG_196:g.242076_242077insGCAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382329.2:c.5662-71_5662-70insGCAT	ENSP00000371766.2:n.5662-71_5662-70insGCAT
ENST00000683406.1:n.2437-71_2437-70insGCAT
ENST00000684637.1:n.1643-71_1643-70insGCAT
ENST00000685949.1:n.4750-71_4750-70insGCAT
ENST00000432829.7:c.5962-71_5962-70insGCAT MANE Select	ENSP00000394888.3:n.5962-71_5962-70insGCAT
ENST00000382329.1:c.4363-71_4363-70insGCAT	ENSP00000371766.1:n.4363-71_4363-70insGCAT
ENST00000432829.6:c.5962-71_5962-70insGCAT	ENSP00000394888.3:n.5962-71_5962-70insGCAT
ENST00000453981.5:c.5758-71_5758-70insGCAT	ENSP00000408464.2:n.5758-71_5758-70insGCAT
ENST00000469391.5:c.5662-71_5662-70insGCAT	ENSP00000419438.1:n.5662-71_5662-70insGCAT
ENST00000495184.5:n.7917-71_7917-70insGCAT
NM_001190458.1:c.5662-71_5662-70insGCAT	NP_001177387.1:n.5662-71_5662-70insGCAT
NM_001193536.1:c.5758-71_5758-70insGCAT	NP_001180465.1:n.5758-71_5758-70insGCAT
NM_203447.3:c.5962-71_5962-70insGCAT , LRG_196t1:c.5962-71_5962-70insGCAT	NP_982272.2:n.5962-71_5962-70insGCAT
XM_011518045.1:c.5662-71_5662-70insGCAT	XP_011516347.1:n.5662-71_5662-70insGCAT
XM_011518046.1:c.5824-71_5824-70insGCAT	XP_011516348.1:n.5824-71_5824-70insGCAT
XM_011518047.1:c.5758-71_5758-70insGCAT	XP_011516349.1:n.5758-71_5758-70insGCAT
XM_011518048.1:c.5758-71_5758-70insGCAT	XP_011516350.1:n.5758-71_5758-70insGCAT
XM_011518049.1:c.4198-71_4198-70insGCAT	XP_011516351.1:n.4198-71_4198-70insGCAT
XM_011518045.3:c.5662-71_5662-70insGCAT	XP_011516347.1:n.5662-71_5662-70insGCAT
XM_011518046.2:c.5824-71_5824-70insGCAT	XP_011516348.1:n.5824-71_5824-70insGCAT
XM_011518047.3:c.5758-71_5758-70insGCAT	XP_011516349.1:n.5758-71_5758-70insGCAT
XM_011518048.2:c.5758-71_5758-70insGCAT	XP_011516350.1:n.5758-71_5758-70insGCAT
XM_011518049.2:c.4198-71_4198-70insGCAT	XP_011516351.1:n.4198-71_4198-70insGCAT
XM_017015173.1:c.5758-71_5758-70insGCAT	XP_016870662.1:n.5758-71_5758-70insGCAT
XM_017015174.1:c.5824-71_5824-70insGCAT	XP_016870663.1:n.5824-71_5824-70insGCAT
NM_001190458.2:c.5662-71_5662-70insGCAT	NP_001177387.1:n.5662-71_5662-70insGCAT
NM_001193536.2:c.5758-71_5758-70insGCAT	NP_001180465.1:n.5758-71_5758-70insGCAT
NM_203447.4:c.5962-71_5962-70insGCAT MANE Select	NP_982272.2:n.5962-71_5962-70insGCAT