Canonical Allele Identifier: CA374657426

Gene: TLR4

Linked Data

• gnomAD v4: 9-117713797-A-G
• MyVariant Identifiers: chr9:g.120476075A>G (hg19) ; chr9:g.117713797A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.117713797A>G , CM000671.2:g.117713797A>G	GRCh38
NC_000009.11:g.120476075A>G , CM000671.1:g.120476075A>G	GRCh37
NC_000009.10:g.119515896A>G	NCBI36
NG_011475.1:g.14616A>G
NG_011475.2:g.14395A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646089.2:c.93+9232A>G	ENSP00000496197.1:n.93+9232A>G
ENST00000697624.1:n.200+9232A>G
ENST00000697625.1:c.93+9232A>G	ENSP00000513362.1:n.93+9232A>G
ENST00000697636.1:c.93+9232A>G	ENSP00000513366.1:n.93+9232A>G
ENST00000697637.1:c.93+9232A>G	ENSP00000513367.1:n.93+9232A>G
ENST00000697664.1:c.140+5068A>G	ENSP00000513389.1:n.140+5068A>G
ENST00000697665.1:c.93+9232A>G	ENSP00000513390.1:n.93+9232A>G
ENST00000697666.1:c.140+5068A>G	ENSP00000513391.1:n.140+5068A>G
ENST00000355622.8:c.1669A>G MANE Select	ENSP00000363089.5:p.Met557Val
ENST00000394487.5:c.1549A>G	ENSP00000377997.4:p.Met517Val
ENST00000472304.2:c.*1403A>G	ENSP00000496429.1:n.*1403A>G
ENST00000642985.1:c.260+5068A>G	ENSP00000493686.1:n.260+5068A>G
ENST00000646089.1:c.93+9232A>G	ENSP00000496197.1:n.93+9232A>G
ENST00000665764.1:c.93+9232A>G	ENSP00000499745.1:n.93+9232A>G
ENST00000355622.6:c.1669A>G	ENSP00000363089.5:p.Met557Val
ENST00000394487.4:c.1549A>G	ENSP00000377997.4:p.Met517Val
ENST00000472304.1:n.1586A>G
NM_003266.3:c.1549A>G	NP_003257.1:p.Met517Val
NM_138554.4:c.1669A>G	NP_612564.1:p.Met557Val
NM_138557.2:c.1069A>G	NP_612567.1:p.Met357Val
NM_138554.5:c.1669A>G MANE Select	NP_612564.1:p.Met557Val
NM_003266.4:c.1549A>G	NP_003257.1:p.Met517Val
NM_138557.3:c.1069A>G	NP_612567.1:p.Met357Val