Canonical Allele Identifier: CA1120385631

Gene: DOCK8

Linked Data

• gnomAD v3: 9-452002-T-TTC
• gnomAD v4: 9-452002-T-TTC

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.452002_452003insTC , CM000671.2:g.452002_452003insTC	GRCh38
NC_000009.11:g.452002_452003insTC , CM000671.1:g.452002_452003insTC	GRCh37
NC_000009.10:g.442002_442003insTC	NCBI36
NG_017007.1:g.242138_242139insTC , LRG_196:g.242138_242139insTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382329.2:c.5662-9_5662-8insTC	ENSP00000371766.2:n.5662-9_5662-8insTC
ENST00000683406.1:n.2437-9_2437-8insTC
ENST00000684637.1:n.1643-9_1643-8insTC
ENST00000685949.1:n.4750-9_4750-8insTC
ENST00000432829.7:c.5962-9_5962-8insTC MANE Select	ENSP00000394888.3:n.5962-9_5962-8insTC
ENST00000382329.1:c.4363-9_4363-8insTC	ENSP00000371766.1:n.4363-9_4363-8insTC
ENST00000432829.6:c.5962-9_5962-8insTC	ENSP00000394888.3:n.5962-9_5962-8insTC
ENST00000453981.5:c.5758-9_5758-8insTC	ENSP00000408464.2:n.5758-9_5758-8insTC
ENST00000469391.5:c.5662-9_5662-8insTC	ENSP00000419438.1:n.5662-9_5662-8insTC
ENST00000495184.5:n.7917-9_7917-8insTC
NM_001190458.1:c.5662-9_5662-8insTC	NP_001177387.1:n.5662-9_5662-8insTC
NM_001193536.1:c.5758-9_5758-8insTC	NP_001180465.1:n.5758-9_5758-8insTC
NM_203447.3:c.5962-9_5962-8insTC , LRG_196t1:c.5962-9_5962-8insTC	NP_982272.2:n.5962-9_5962-8insTC
XM_011518045.1:c.5662-9_5662-8insTC	XP_011516347.1:n.5662-9_5662-8insTC
XM_011518046.1:c.5824-9_5824-8insTC	XP_011516348.1:n.5824-9_5824-8insTC
XM_011518047.1:c.5758-9_5758-8insTC	XP_011516349.1:n.5758-9_5758-8insTC
XM_011518048.1:c.5758-9_5758-8insTC	XP_011516350.1:n.5758-9_5758-8insTC
XM_011518049.1:c.4198-9_4198-8insTC	XP_011516351.1:n.4198-9_4198-8insTC
XM_011518045.3:c.5662-9_5662-8insTC	XP_011516347.1:n.5662-9_5662-8insTC
XM_011518046.2:c.5824-9_5824-8insTC	XP_011516348.1:n.5824-9_5824-8insTC
XM_011518047.3:c.5758-9_5758-8insTC	XP_011516349.1:n.5758-9_5758-8insTC
XM_011518048.2:c.5758-9_5758-8insTC	XP_011516350.1:n.5758-9_5758-8insTC
XM_011518049.2:c.4198-9_4198-8insTC	XP_011516351.1:n.4198-9_4198-8insTC
XM_017015173.1:c.5758-9_5758-8insTC	XP_016870662.1:n.5758-9_5758-8insTC
XM_017015174.1:c.5824-9_5824-8insTC	XP_016870663.1:n.5824-9_5824-8insTC
NM_001190458.2:c.5662-9_5662-8insTC	NP_001177387.1:n.5662-9_5662-8insTC
NM_001193536.2:c.5758-9_5758-8insTC	NP_001180465.1:n.5758-9_5758-8insTC
NM_203447.4:c.5962-9_5962-8insTC MANE Select	NP_982272.2:n.5962-9_5962-8insTC