Canonical Allele Identifier: CA859260688

Gene: TLR4

Linked Data

• dbSNP Id: rs987483402
• gnomAD v3: 9-117721806-G-A
• gnomAD v4: 9-117721806-G-A
• MyVariant Identifiers: chr9:g.120484084G>A (hg19) ; chr9:g.117721806G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.117721806G>A , CM000671.2:g.117721806G>A	GRCh38
NC_000009.11:g.120484084G>A , CM000671.1:g.120484084G>A	GRCh37
NC_000009.10:g.119523905G>A	NCBI36
NG_011475.2:g.22404G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646089.2:c.93+17241G>A	ENSP00000496197.1:n.93+17241G>A
ENST00000697624.1:n.200+17241G>A
ENST00000697625.1:c.93+17241G>A	ENSP00000513362.1:n.93+17241G>A
ENST00000697636.1:c.93+17241G>A	ENSP00000513366.1:n.93+17241G>A
ENST00000697637.1:c.93+17241G>A	ENSP00000513367.1:n.93+17241G>A
ENST00000697664.1:c.140+13077G>A	ENSP00000513389.1:n.140+13077G>A
ENST00000697665.1:c.93+17241G>A	ENSP00000513390.1:n.93+17241G>A
ENST00000697666.1:c.140+13077G>A	ENSP00000513391.1:n.140+13077G>A
ENST00000355622.8:c.*7158G>A MANE Select	ENSP00000363089.5:n.*7158G>A
ENST00000642985.1:c.260+13077G>A	ENSP00000493686.1:n.260+13077G>A
ENST00000646089.1:c.93+17241G>A	ENSP00000496197.1:n.93+17241G>A
ENST00000665764.1:c.93+17241G>A	ENSP00000499745.1:n.93+17241G>A
NM_138554.5:c.*7158G>A MANE Select	NP_612564.1:n.*7158G>A
NM_003266.4:c.*7158G>A	NP_003257.1:n.*7158G>A
NM_138557.3:c.*7158G>A	NP_612567.1:n.*7158G>A