Canonical Allele Identifier: CA1826910270

Gene: DOCK8

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.451787_451791delinsAAACT , CM000671.2:g.451787_451791delinsAAACT	GRCh38
NC_000009.11:g.451787_451791delinsAAACT , CM000671.1:g.451787_451791delinsAAACT	GRCh37
NC_000009.10:g.441787_441791delinsAAACT	NCBI36
NG_017007.1:g.241923_241927delinsAAACT , LRG_196:g.241923_241927delinsAAACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382329.2:c.5662-224_5662-220delinsAAACT	ENSP00000371766.2:n.5662-224_5662-220delinsAAACT
ENST00000683406.1:n.2437-224_2437-220delinsAAACT
ENST00000684637.1:n.1643-224_1643-220delinsAAACT
ENST00000685949.1:n.4750-224_4750-220delinsAAACT
ENST00000432829.7:c.5962-224_5962-220delinsAAACT MANE Select	ENSP00000394888.3:n.5962-224_5962-220delinsAAACT
ENST00000382329.1:c.4363-224_4363-220delinsAAACT	ENSP00000371766.1:n.4363-224_4363-220delinsAAACT
ENST00000432829.6:c.5962-224_5962-220delinsAAACT	ENSP00000394888.3:n.5962-224_5962-220delinsAAACT
ENST00000453981.5:c.5758-224_5758-220delinsAAACT	ENSP00000408464.2:n.5758-224_5758-220delinsAAACT
ENST00000469391.5:c.5662-224_5662-220delinsAAACT	ENSP00000419438.1:n.5662-224_5662-220delinsAAACT
ENST00000495184.5:n.7917-224_7917-220delinsAAACT
NM_001190458.1:c.5662-224_5662-220delinsAAACT	NP_001177387.1:n.5662-224_5662-220delinsAAACT
NM_001193536.1:c.5758-224_5758-220delinsAAACT	NP_001180465.1:n.5758-224_5758-220delinsAAACT
NM_203447.3:c.5962-224_5962-220delinsAAACT , LRG_196t1:c.5962-224_5962-220delinsAAACT	NP_982272.2:n.5962-224_5962-220delinsAAACT
XM_011518045.1:c.5662-224_5662-220delinsAAACT	XP_011516347.1:n.5662-224_5662-220delinsAAACT
XM_011518046.1:c.5824-224_5824-220delinsAAACT	XP_011516348.1:n.5824-224_5824-220delinsAAACT
XM_011518047.1:c.5758-224_5758-220delinsAAACT	XP_011516349.1:n.5758-224_5758-220delinsAAACT
XM_011518048.1:c.5758-224_5758-220delinsAAACT	XP_011516350.1:n.5758-224_5758-220delinsAAACT
XM_011518049.1:c.4198-224_4198-220delinsAAACT	XP_011516351.1:n.4198-224_4198-220delinsAAACT
XM_011518045.3:c.5662-224_5662-220delinsAAACT	XP_011516347.1:n.5662-224_5662-220delinsAAACT
XM_011518046.2:c.5824-224_5824-220delinsAAACT	XP_011516348.1:n.5824-224_5824-220delinsAAACT
XM_011518047.3:c.5758-224_5758-220delinsAAACT	XP_011516349.1:n.5758-224_5758-220delinsAAACT
XM_011518048.2:c.5758-224_5758-220delinsAAACT	XP_011516350.1:n.5758-224_5758-220delinsAAACT
XM_011518049.2:c.4198-224_4198-220delinsAAACT	XP_011516351.1:n.4198-224_4198-220delinsAAACT
XM_017015173.1:c.5758-224_5758-220delinsAAACT	XP_016870662.1:n.5758-224_5758-220delinsAAACT
XM_017015174.1:c.5824-224_5824-220delinsAAACT	XP_016870663.1:n.5824-224_5824-220delinsAAACT
NM_001190458.2:c.5662-224_5662-220delinsAAACT	NP_001177387.1:n.5662-224_5662-220delinsAAACT
NM_001193536.2:c.5758-224_5758-220delinsAAACT	NP_001180465.1:n.5758-224_5758-220delinsAAACT
NM_203447.4:c.5962-224_5962-220delinsAAACT MANE Select	NP_982272.2:n.5962-224_5962-220delinsAAACT