Canonical Allele Identifier: CA5212406

Gene: TLR4

Linked Data

• dbSNP Id: rs762384409
• ExAC: 9:120476081 T / C
• gnomAD v2: 9-120476081-T-C
• MyVariant Identifiers: chr9:g.120476081T>C (hg19) ; chr9:g.117713803T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.117713803T>C , CM000671.2:g.117713803T>C	GRCh38
NC_000009.11:g.120476081T>C , CM000671.1:g.120476081T>C	GRCh37
NC_000009.10:g.119515902T>C	NCBI36
NG_011475.1:g.14622T>C
NG_011475.2:g.14401T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646089.2:c.93+9238T>C	ENSP00000496197.1:n.93+9238T>C
ENST00000697624.1:n.200+9238T>C
ENST00000697625.1:c.93+9238T>C	ENSP00000513362.1:n.93+9238T>C
ENST00000697636.1:c.93+9238T>C	ENSP00000513366.1:n.93+9238T>C
ENST00000697637.1:c.93+9238T>C	ENSP00000513367.1:n.93+9238T>C
ENST00000697664.1:c.140+5074T>C	ENSP00000513389.1:n.140+5074T>C
ENST00000697665.1:c.93+9238T>C	ENSP00000513390.1:n.93+9238T>C
ENST00000697666.1:c.140+5074T>C	ENSP00000513391.1:n.140+5074T>C
ENST00000355622.8:c.1675T>C MANE Select	ENSP00000363089.5:p.Ser559Pro
ENST00000394487.5:c.1555T>C	ENSP00000377997.4:p.Ser519Pro
ENST00000472304.2:c.*1409T>C	ENSP00000496429.1:n.*1409T>C
ENST00000642985.1:c.260+5074T>C	ENSP00000493686.1:n.260+5074T>C
ENST00000646089.1:c.93+9238T>C	ENSP00000496197.1:n.93+9238T>C
ENST00000665764.1:c.93+9238T>C	ENSP00000499745.1:n.93+9238T>C
ENST00000355622.6:c.1675T>C	ENSP00000363089.5:p.Ser559Pro
ENST00000394487.4:c.1555T>C	ENSP00000377997.4:p.Ser519Pro
ENST00000472304.1:n.1592T>C
NM_003266.3:c.1555T>C	NP_003257.1:p.Ser519Pro
NM_138554.4:c.1675T>C	NP_612564.1:p.Ser559Pro
NM_138557.2:c.1075T>C	NP_612567.1:p.Ser359Pro
NM_138554.5:c.1675T>C MANE Select	NP_612564.1:p.Ser559Pro
NM_003266.4:c.1555T>C	NP_003257.1:p.Ser519Pro
NM_138557.3:c.1075T>C	NP_612567.1:p.Ser359Pro