Canonical Allele Identifier: CA1120385488

Gene: DOCK8

Linked Data

• gnomAD v3: 9-451975-A-ATTTTT
• gnomAD v4: 9-451975-A-ATTTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.451976_451977insTTTTT , CM000671.2:g.451976_451977insTTTTT	GRCh38
NC_000009.11:g.451976_451977insTTTTT , CM000671.1:g.451976_451977insTTTTT	GRCh37
NC_000009.10:g.441976_441977insTTTTT	NCBI36
NG_017007.1:g.242112_242113insTTTTT , LRG_196:g.242112_242113insTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382329.2:c.5662-35_5662-34insTTTTT	ENSP00000371766.2:n.5662-35_5662-34insTTTTT
ENST00000683406.1:n.2437-35_2437-34insTTTTT
ENST00000684637.1:n.1643-35_1643-34insTTTTT
ENST00000685949.1:n.4750-35_4750-34insTTTTT
ENST00000432829.7:c.5962-35_5962-34insTTTTT MANE Select	ENSP00000394888.3:n.5962-35_5962-34insTTTTT
ENST00000382329.1:c.4363-35_4363-34insTTTTT	ENSP00000371766.1:n.4363-35_4363-34insTTTTT
ENST00000432829.6:c.5962-35_5962-34insTTTTT	ENSP00000394888.3:n.5962-35_5962-34insTTTTT
ENST00000453981.5:c.5758-35_5758-34insTTTTT	ENSP00000408464.2:n.5758-35_5758-34insTTTTT
ENST00000469391.5:c.5662-35_5662-34insTTTTT	ENSP00000419438.1:n.5662-35_5662-34insTTTTT
ENST00000495184.5:n.7917-35_7917-34insTTTTT
NM_001190458.1:c.5662-35_5662-34insTTTTT	NP_001177387.1:n.5662-35_5662-34insTTTTT
NM_001193536.1:c.5758-35_5758-34insTTTTT	NP_001180465.1:n.5758-35_5758-34insTTTTT
NM_203447.3:c.5962-35_5962-34insTTTTT , LRG_196t1:c.5962-35_5962-34insTTTTT	NP_982272.2:n.5962-35_5962-34insTTTTT
XM_011518045.1:c.5662-35_5662-34insTTTTT	XP_011516347.1:n.5662-35_5662-34insTTTTT
XM_011518046.1:c.5824-35_5824-34insTTTTT	XP_011516348.1:n.5824-35_5824-34insTTTTT
XM_011518047.1:c.5758-35_5758-34insTTTTT	XP_011516349.1:n.5758-35_5758-34insTTTTT
XM_011518048.1:c.5758-35_5758-34insTTTTT	XP_011516350.1:n.5758-35_5758-34insTTTTT
XM_011518049.1:c.4198-35_4198-34insTTTTT	XP_011516351.1:n.4198-35_4198-34insTTTTT
XM_011518045.3:c.5662-35_5662-34insTTTTT	XP_011516347.1:n.5662-35_5662-34insTTTTT
XM_011518046.2:c.5824-35_5824-34insTTTTT	XP_011516348.1:n.5824-35_5824-34insTTTTT
XM_011518047.3:c.5758-35_5758-34insTTTTT	XP_011516349.1:n.5758-35_5758-34insTTTTT
XM_011518048.2:c.5758-35_5758-34insTTTTT	XP_011516350.1:n.5758-35_5758-34insTTTTT
XM_011518049.2:c.4198-35_4198-34insTTTTT	XP_011516351.1:n.4198-35_4198-34insTTTTT
XM_017015173.1:c.5758-35_5758-34insTTTTT	XP_016870662.1:n.5758-35_5758-34insTTTTT
XM_017015174.1:c.5824-35_5824-34insTTTTT	XP_016870663.1:n.5824-35_5824-34insTTTTT
NM_001190458.2:c.5662-35_5662-34insTTTTT	NP_001177387.1:n.5662-35_5662-34insTTTTT
NM_001193536.2:c.5758-35_5758-34insTTTTT	NP_001180465.1:n.5758-35_5758-34insTTTTT
NM_203447.4:c.5962-35_5962-34insTTTTT MANE Select	NP_982272.2:n.5962-35_5962-34insTTTTT