Canonical Allele Identifier: CA374656917

Gene: TLR4

Linked Data

• gnomAD v4: 9-117713573-C-G
• MyVariant Identifiers: chr9:g.120475851C>G (hg19) ; chr9:g.117713573C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.117713573C>G , CM000671.2:g.117713573C>G	GRCh38
NC_000009.11:g.120475851C>G , CM000671.1:g.120475851C>G	GRCh37
NC_000009.10:g.119515672C>G	NCBI36
NG_011475.1:g.14392C>G
NG_011475.2:g.14171C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646089.2:c.93+9008C>G	ENSP00000496197.1:n.93+9008C>G
ENST00000697624.1:n.200+9008C>G
ENST00000697625.1:c.93+9008C>G	ENSP00000513362.1:n.93+9008C>G
ENST00000697636.1:c.93+9008C>G	ENSP00000513366.1:n.93+9008C>G
ENST00000697637.1:c.93+9008C>G	ENSP00000513367.1:n.93+9008C>G
ENST00000697664.1:c.140+4844C>G	ENSP00000513389.1:n.140+4844C>G
ENST00000697665.1:c.93+9008C>G	ENSP00000513390.1:n.93+9008C>G
ENST00000697666.1:c.140+4844C>G	ENSP00000513391.1:n.140+4844C>G
ENST00000355622.8:c.1445C>G MANE Select	ENSP00000363089.5:p.Ser482Cys
ENST00000394487.5:c.1325C>G	ENSP00000377997.4:p.Ser442Cys
ENST00000472304.2:c.*1179C>G	ENSP00000496429.1:n.*1179C>G
ENST00000642985.1:c.260+4844C>G	ENSP00000493686.1:n.260+4844C>G
ENST00000646089.1:c.93+9008C>G	ENSP00000496197.1:n.93+9008C>G
ENST00000665764.1:c.93+9008C>G	ENSP00000499745.1:n.93+9008C>G
ENST00000355622.6:c.1445C>G	ENSP00000363089.5:p.Ser482Cys
ENST00000394487.4:c.1325C>G	ENSP00000377997.4:p.Ser442Cys
ENST00000472304.1:n.1362C>G
NM_003266.3:c.1325C>G	NP_003257.1:p.Ser442Cys
NM_138554.4:c.1445C>G	NP_612564.1:p.Ser482Cys
NM_138557.2:c.845C>G	NP_612567.1:p.Ser282Cys
NM_138554.5:c.1445C>G MANE Select	NP_612564.1:p.Ser482Cys
NM_003266.4:c.1325C>G	NP_003257.1:p.Ser442Cys
NM_138557.3:c.845C>G	NP_612567.1:p.Ser282Cys