Canonical Allele Identifier: CA198764342
Gene: TLR4 HGNC NCBI

Linked Data

dbSNP Id: rs1057317
gnomAD v4: 9-117715764-C-A
MyVariant Identifiers: chr9:g.120478042C>A (hg19) chr9:g.117715764C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.117715764C>A , CM000671.2:g.117715764C>A GRCh38
NC_000009.11:g.120478042C>A , CM000671.1:g.120478042C>A GRCh37
NC_000009.10:g.119517863C>A NCBI36
NG_011475.1:g.16583C>A
NG_011475.2:g.16362C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000646089.2:c.93+11199C>A ENSP00000496197.1:n.93+11199C>A
ENST00000697624.1:n.200+11199C>A
ENST00000697625.1:c.93+11199C>A ENSP00000513362.1:n.93+11199C>A
ENST00000697636.1:c.93+11199C>A ENSP00000513366.1:n.93+11199C>A
ENST00000697637.1:c.93+11199C>A ENSP00000513367.1:n.93+11199C>A
ENST00000697664.1:c.140+7035C>A ENSP00000513389.1:n.140+7035C>A
ENST00000697665.1:c.93+11199C>A ENSP00000513390.1:n.93+11199C>A
ENST00000697666.1:c.140+7035C>A ENSP00000513391.1:n.140+7035C>A
ENST00000355622.8:c.*1116C>A MANE Select ENSP00000363089.5:n.*1116C>A
ENST00000394487.5:c.*1116C>A ENSP00000377997.4:n.*1116C>A
ENST00000642985.1:c.260+7035C>A ENSP00000493686.1:n.260+7035C>A
ENST00000646089.1:c.93+11199C>A ENSP00000496197.1:n.93+11199C>A
ENST00000665764.1:c.93+11199C>A ENSP00000499745.1:n.93+11199C>A
ENST00000355622.6:c.*1116C>A ENSP00000363089.5:n.*1116C>A
ENST00000394487.4:c.*1116C>A ENSP00000377997.4:n.*1116C>A
NM_003266.3:c.*1116C>A NP_003257.1:n.*1116C>A
NM_138554.4:c.*1116C>A NP_612564.1:n.*1116C>A
NM_138557.2:c.*1116C>A NP_612567.1:n.*1116C>A
NM_138554.5:c.*1116C>A MANE Select NP_612564.1:n.*1116C>A
NM_003266.4:c.*1116C>A NP_003257.1:n.*1116C>A
NM_138557.3:c.*1116C>A NP_612567.1:n.*1116C>A
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