Canonical Allele Identifier: CA374656462

Gene: TLR4

Linked Data

• gnomAD v4: 9-117713371-A-C
• MyVariant Identifiers: chr9:g.120475649A>C (hg19) ; chr9:g.117713371A>C (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646089.2:c.93+8806A>C	ENSP00000496197.1:n.93+8806A>C
ENST00000697624.1:n.200+8806A>C
ENST00000697625.1:c.93+8806A>C	ENSP00000513362.1:n.93+8806A>C
ENST00000697636.1:c.93+8806A>C	ENSP00000513366.1:n.93+8806A>C
ENST00000697637.1:c.93+8806A>C	ENSP00000513367.1:n.93+8806A>C
ENST00000697664.1:c.140+4642A>C	ENSP00000513389.1:n.140+4642A>C
ENST00000697665.1:c.93+8806A>C	ENSP00000513390.1:n.93+8806A>C
ENST00000697666.1:c.140+4642A>C	ENSP00000513391.1:n.140+4642A>C
ENST00000355622.8:c.1243A>C MANE Select	ENSP00000363089.5:p.Ser415Arg
ENST00000394487.5:c.1123A>C	ENSP00000377997.4:p.Ser375Arg
ENST00000472304.2:c.*977A>C	ENSP00000496429.1:n.*977A>C
ENST00000642985.1:c.260+4642A>C	ENSP00000493686.1:n.260+4642A>C
ENST00000646089.1:c.93+8806A>C	ENSP00000496197.1:n.93+8806A>C
ENST00000665764.1:c.93+8806A>C	ENSP00000499745.1:n.93+8806A>C
ENST00000355622.6:c.1243A>C	ENSP00000363089.5:p.Ser415Arg
ENST00000394487.4:c.1123A>C	ENSP00000377997.4:p.Ser375Arg
ENST00000472304.1:n.1160A>C
NM_003266.3:c.1123A>C	NP_003257.1:p.Ser375Arg
NM_138554.4:c.1243A>C	NP_612564.1:p.Ser415Arg
NM_138557.2:c.643A>C	NP_612567.1:p.Ser215Arg
NM_138554.5:c.1243A>C MANE Select	NP_612564.1:p.Ser415Arg
NM_003266.4:c.1123A>C	NP_003257.1:p.Ser375Arg
NM_138557.3:c.643A>C	NP_612567.1:p.Ser215Arg