Canonical Allele Identifier: CA1826910312

Gene: DOCK8

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.451863_451867delinsATGTG , CM000671.2:g.451863_451867delinsATGTG	GRCh38
NC_000009.11:g.451863_451867delinsATGTG , CM000671.1:g.451863_451867delinsATGTG	GRCh37
NC_000009.10:g.441863_441867delinsATGTG	NCBI36
NG_017007.1:g.241999_242003delinsATGTG , LRG_196:g.241999_242003delinsATGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382329.2:c.5662-148_5662-144delinsATGTG	ENSP00000371766.2:n.5662-148_5662-144delinsATGTG
ENST00000683406.1:n.2437-148_2437-144delinsATGTG
ENST00000684637.1:n.1643-148_1643-144delinsATGTG
ENST00000685949.1:n.4750-148_4750-144delinsATGTG
ENST00000432829.7:c.5962-148_5962-144delinsATGTG MANE Select	ENSP00000394888.3:n.5962-148_5962-144delinsATGTG
ENST00000382329.1:c.4363-148_4363-144delinsATGTG	ENSP00000371766.1:n.4363-148_4363-144delinsATGTG
ENST00000432829.6:c.5962-148_5962-144delinsATGTG	ENSP00000394888.3:n.5962-148_5962-144delinsATGTG
ENST00000453981.5:c.5758-148_5758-144delinsATGTG	ENSP00000408464.2:n.5758-148_5758-144delinsATGTG
ENST00000469391.5:c.5662-148_5662-144delinsATGTG	ENSP00000419438.1:n.5662-148_5662-144delinsATGTG
ENST00000495184.5:n.7917-148_7917-144delinsATGTG
NM_001190458.1:c.5662-148_5662-144delinsATGTG	NP_001177387.1:n.5662-148_5662-144delinsATGTG
NM_001193536.1:c.5758-148_5758-144delinsATGTG	NP_001180465.1:n.5758-148_5758-144delinsATGTG
NM_203447.3:c.5962-148_5962-144delinsATGTG , LRG_196t1:c.5962-148_5962-144delinsATGTG	NP_982272.2:n.5962-148_5962-144delinsATGTG
XM_011518045.1:c.5662-148_5662-144delinsATGTG	XP_011516347.1:n.5662-148_5662-144delinsATGTG
XM_011518046.1:c.5824-148_5824-144delinsATGTG	XP_011516348.1:n.5824-148_5824-144delinsATGTG
XM_011518047.1:c.5758-148_5758-144delinsATGTG	XP_011516349.1:n.5758-148_5758-144delinsATGTG
XM_011518048.1:c.5758-148_5758-144delinsATGTG	XP_011516350.1:n.5758-148_5758-144delinsATGTG
XM_011518049.1:c.4198-148_4198-144delinsATGTG	XP_011516351.1:n.4198-148_4198-144delinsATGTG
XM_011518045.3:c.5662-148_5662-144delinsATGTG	XP_011516347.1:n.5662-148_5662-144delinsATGTG
XM_011518046.2:c.5824-148_5824-144delinsATGTG	XP_011516348.1:n.5824-148_5824-144delinsATGTG
XM_011518047.3:c.5758-148_5758-144delinsATGTG	XP_011516349.1:n.5758-148_5758-144delinsATGTG
XM_011518048.2:c.5758-148_5758-144delinsATGTG	XP_011516350.1:n.5758-148_5758-144delinsATGTG
XM_011518049.2:c.4198-148_4198-144delinsATGTG	XP_011516351.1:n.4198-148_4198-144delinsATGTG
XM_017015173.1:c.5758-148_5758-144delinsATGTG	XP_016870662.1:n.5758-148_5758-144delinsATGTG
XM_017015174.1:c.5824-148_5824-144delinsATGTG	XP_016870663.1:n.5824-148_5824-144delinsATGTG
NM_001190458.2:c.5662-148_5662-144delinsATGTG	NP_001177387.1:n.5662-148_5662-144delinsATGTG
NM_001193536.2:c.5758-148_5758-144delinsATGTG	NP_001180465.1:n.5758-148_5758-144delinsATGTG
NM_203447.4:c.5962-148_5962-144delinsATGTG MANE Select	NP_982272.2:n.5962-148_5962-144delinsATGTG