Canonical Allele Identifier: CA590172086

Gene: TLR4

Linked Data

• dbSNP Id: rs1192251644
• gnomAD v2: 9-120484028-AATT-A
• gnomAD v3: 9-117721750-AATT-A
• gnomAD v4: 9-117721750-AATT-A
• MyVariant Identifiers: chr9:g.120484029_120484031del (hg19) ; chr9:g.117721751_117721753del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.117721752_117721754del , CM000671.2:g.117721752_117721754del	GRCh38
NC_000009.11:g.120484030_120484032del , CM000671.1:g.120484030_120484032del	GRCh37
NC_000009.10:g.119523851_119523853del	NCBI36
NG_011475.2:g.22350_22352del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646089.2:c.93+17187_93+17189del	ENSP00000496197.1:n.93+17187_93+17189del
ENST00000697624.1:n.200+17187_200+17189del
ENST00000697625.1:c.93+17187_93+17189del	ENSP00000513362.1:n.93+17187_93+17189del
ENST00000697636.1:c.93+17187_93+17189del	ENSP00000513366.1:n.93+17187_93+17189del
ENST00000697637.1:c.93+17187_93+17189del	ENSP00000513367.1:n.93+17187_93+17189del
ENST00000697664.1:c.140+13023_140+13025del	ENSP00000513389.1:n.140+13023_140+13025del
ENST00000697665.1:c.93+17187_93+17189del	ENSP00000513390.1:n.93+17187_93+17189del
ENST00000697666.1:c.140+13023_140+13025del	ENSP00000513391.1:n.140+13023_140+13025del
ENST00000355622.8:c.*7104_*7106del MANE Select	ENSP00000363089.5:n.*7104_*7106del
ENST00000642985.1:c.260+13023_260+13025del	ENSP00000493686.1:n.260+13023_260+13025del
ENST00000646089.1:c.93+17187_93+17189del	ENSP00000496197.1:n.93+17187_93+17189del
ENST00000665764.1:c.93+17187_93+17189del	ENSP00000499745.1:n.93+17187_93+17189del
NM_138554.5:c.*7104_*7106del MANE Select	NP_612564.1:n.*7104_*7106del
NM_003266.4:c.*7104_*7106del	NP_003257.1:n.*7104_*7106del
NM_138557.3:c.*7104_*7106del	NP_612567.1:n.*7104_*7106del