Canonical Allele Identifier: CA859260576

Gene: TLR4

Linked Data

• dbSNP Id: rs1288286175
• MyVariant Identifiers: chr9:g.120483918_120483923del (hg19) ; chr9:g.117721640_117721645del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.117721643_117721648del , CM000671.2:g.117721643_117721648del	GRCh38
NC_000009.11:g.120483921_120483926del , CM000671.1:g.120483921_120483926del	GRCh37
NC_000009.10:g.119523742_119523747del	NCBI36
NG_011475.2:g.22241_22246del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646089.2:c.93+17078_93+17083del	ENSP00000496197.1:n.93+17078_93+17083del
ENST00000697624.1:n.200+17078_200+17083del
ENST00000697625.1:c.93+17078_93+17083del	ENSP00000513362.1:n.93+17078_93+17083del
ENST00000697636.1:c.93+17078_93+17083del	ENSP00000513366.1:n.93+17078_93+17083del
ENST00000697637.1:c.93+17078_93+17083del	ENSP00000513367.1:n.93+17078_93+17083del
ENST00000697664.1:c.140+12914_140+12919del	ENSP00000513389.1:n.140+12914_140+12919del
ENST00000697665.1:c.93+17078_93+17083del	ENSP00000513390.1:n.93+17078_93+17083del
ENST00000697666.1:c.140+12914_140+12919del	ENSP00000513391.1:n.140+12914_140+12919del
ENST00000355622.8:c.*6995_*7000del MANE Select	ENSP00000363089.5:n.*6995_*7000del
ENST00000642985.1:c.260+12914_260+12919del	ENSP00000493686.1:n.260+12914_260+12919del
ENST00000646089.1:c.93+17078_93+17083del	ENSP00000496197.1:n.93+17078_93+17083del
ENST00000665764.1:c.93+17078_93+17083del	ENSP00000499745.1:n.93+17078_93+17083del
NM_138554.5:c.*6995_*7000del MANE Select	NP_612564.1:n.*6995_*7000del
NM_003266.4:c.*6995_*7000del	NP_003257.1:n.*6995_*7000del
NM_138557.3:c.*6995_*7000del	NP_612567.1:n.*6995_*7000del