Canonical Allele Identifier: CA374656463

Gene: TLR4

Linked Data

• COSMIC: COSM1267925
• MyVariant Identifiers: chr9:g.120475649A>G (hg19) ; chr9:g.117713371A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.117713371A>G , CM000671.2:g.117713371A>G	GRCh38
NC_000009.11:g.120475649A>G , CM000671.1:g.120475649A>G	GRCh37
NC_000009.10:g.119515470A>G	NCBI36
NG_011475.1:g.14190A>G
NG_011475.2:g.13969A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646089.2:c.93+8806A>G	ENSP00000496197.1:n.93+8806A>G
ENST00000697624.1:n.200+8806A>G
ENST00000697625.1:c.93+8806A>G	ENSP00000513362.1:n.93+8806A>G
ENST00000697636.1:c.93+8806A>G	ENSP00000513366.1:n.93+8806A>G
ENST00000697637.1:c.93+8806A>G	ENSP00000513367.1:n.93+8806A>G
ENST00000697664.1:c.140+4642A>G	ENSP00000513389.1:n.140+4642A>G
ENST00000697665.1:c.93+8806A>G	ENSP00000513390.1:n.93+8806A>G
ENST00000697666.1:c.140+4642A>G	ENSP00000513391.1:n.140+4642A>G
ENST00000355622.8:c.1243A>G MANE Select	ENSP00000363089.5:p.Ser415Gly
ENST00000394487.5:c.1123A>G	ENSP00000377997.4:p.Ser375Gly
ENST00000472304.2:c.*977A>G	ENSP00000496429.1:n.*977A>G
ENST00000642985.1:c.260+4642A>G	ENSP00000493686.1:n.260+4642A>G
ENST00000646089.1:c.93+8806A>G	ENSP00000496197.1:n.93+8806A>G
ENST00000665764.1:c.93+8806A>G	ENSP00000499745.1:n.93+8806A>G
ENST00000355622.6:c.1243A>G	ENSP00000363089.5:p.Ser415Gly
ENST00000394487.4:c.1123A>G	ENSP00000377997.4:p.Ser375Gly
ENST00000472304.1:n.1160A>G
NM_003266.3:c.1123A>G	NP_003257.1:p.Ser375Gly
NM_138554.4:c.1243A>G	NP_612564.1:p.Ser415Gly
NM_138557.2:c.643A>G	NP_612567.1:p.Ser215Gly
NM_138554.5:c.1243A>G MANE Select	NP_612564.1:p.Ser415Gly
NM_003266.4:c.1123A>G	NP_003257.1:p.Ser375Gly
NM_138557.3:c.643A>G	NP_612567.1:p.Ser215Gly