Canonical Allele Identifier: CA864780135

Gene: DOCK8

Linked Data

• dbSNP Id: rs1229148474
• gnomAD v3: 9-451871-GTATATATATATACATA-G
• gnomAD v4: 9-451871-GTATATATATATACATA-G
• MyVariant Identifiers: chr9:g.451872_451887del (hg19) ; chr9:g.451872_451887del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.451877_451892del , CM000671.2:g.451877_451892del	GRCh38
NC_000009.11:g.451877_451892del , CM000671.1:g.451877_451892del	GRCh37
NC_000009.10:g.441877_441892del	NCBI36
NG_017007.1:g.242013_242028del , LRG_196:g.242013_242028del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382329.2:c.5662-134_5662-119del	ENSP00000371766.2:n.5662-134_5662-119del
ENST00000683406.1:n.2437-134_2437-119del
ENST00000684637.1:n.1643-134_1643-119del
ENST00000685949.1:n.4750-134_4750-119del
ENST00000432829.7:c.5962-134_5962-119del MANE Select	ENSP00000394888.3:n.5962-134_5962-119del
ENST00000382329.1:c.4363-134_4363-119del	ENSP00000371766.1:n.4363-134_4363-119del
ENST00000432829.6:c.5962-134_5962-119del	ENSP00000394888.3:n.5962-134_5962-119del
ENST00000453981.5:c.5758-134_5758-119del	ENSP00000408464.2:n.5758-134_5758-119del
ENST00000469391.5:c.5662-134_5662-119del	ENSP00000419438.1:n.5662-134_5662-119del
ENST00000495184.5:n.7917-134_7917-119del
NM_001190458.1:c.5662-134_5662-119del	NP_001177387.1:n.5662-134_5662-119del
NM_001193536.1:c.5758-134_5758-119del	NP_001180465.1:n.5758-134_5758-119del
NM_203447.3:c.5962-134_5962-119del , LRG_196t1:c.5962-134_5962-119del	NP_982272.2:n.5962-134_5962-119del
XM_011518045.1:c.5662-134_5662-119del	XP_011516347.1:n.5662-134_5662-119del
XM_011518046.1:c.5824-134_5824-119del	XP_011516348.1:n.5824-134_5824-119del
XM_011518047.1:c.5758-134_5758-119del	XP_011516349.1:n.5758-134_5758-119del
XM_011518048.1:c.5758-134_5758-119del	XP_011516350.1:n.5758-134_5758-119del
XM_011518049.1:c.4198-134_4198-119del	XP_011516351.1:n.4198-134_4198-119del
XM_011518045.3:c.5662-134_5662-119del	XP_011516347.1:n.5662-134_5662-119del
XM_011518046.2:c.5824-134_5824-119del	XP_011516348.1:n.5824-134_5824-119del
XM_011518047.3:c.5758-134_5758-119del	XP_011516349.1:n.5758-134_5758-119del
XM_011518048.2:c.5758-134_5758-119del	XP_011516350.1:n.5758-134_5758-119del
XM_011518049.2:c.4198-134_4198-119del	XP_011516351.1:n.4198-134_4198-119del
XM_017015173.1:c.5758-134_5758-119del	XP_016870662.1:n.5758-134_5758-119del
XM_017015174.1:c.5824-134_5824-119del	XP_016870663.1:n.5824-134_5824-119del
NM_001190458.2:c.5662-134_5662-119del	NP_001177387.1:n.5662-134_5662-119del
NM_001193536.2:c.5758-134_5758-119del	NP_001180465.1:n.5758-134_5758-119del
NM_203447.4:c.5962-134_5962-119del MANE Select	NP_982272.2:n.5962-134_5962-119del