Canonical Allele Identifier: CA374656140

Gene: TLR4

Linked Data

• gnomAD v4: 9-117713225-C-A
• MyVariant Identifiers: chr9:g.120475503C>A (hg19) ; chr9:g.117713225C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.117713225C>A , CM000671.2:g.117713225C>A	GRCh38
NC_000009.11:g.120475503C>A , CM000671.1:g.120475503C>A	GRCh37
NC_000009.10:g.119515324C>A	NCBI36
NG_011475.1:g.14044C>A
NG_011475.2:g.13823C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000646089.2:c.93+8660C>A	ENSP00000496197.1:n.93+8660C>A
ENST00000697624.1:n.200+8660C>A
ENST00000697625.1:c.93+8660C>A	ENSP00000513362.1:n.93+8660C>A
ENST00000697636.1:c.93+8660C>A	ENSP00000513366.1:n.93+8660C>A
ENST00000697637.1:c.93+8660C>A	ENSP00000513367.1:n.93+8660C>A
ENST00000697664.1:c.140+4496C>A	ENSP00000513389.1:n.140+4496C>A
ENST00000697665.1:c.93+8660C>A	ENSP00000513390.1:n.93+8660C>A
ENST00000697666.1:c.140+4496C>A	ENSP00000513391.1:n.140+4496C>A
ENST00000355622.8:c.1097C>A MANE Select	ENSP00000363089.5:p.Ala366Asp
ENST00000394487.5:c.977C>A	ENSP00000377997.4:p.Ala326Asp
ENST00000472304.2:c.*831C>A	ENSP00000496429.1:n.*831C>A
ENST00000642985.1:c.260+4496C>A	ENSP00000493686.1:n.260+4496C>A
ENST00000646089.1:c.93+8660C>A	ENSP00000496197.1:n.93+8660C>A
ENST00000665764.1:c.93+8660C>A	ENSP00000499745.1:n.93+8660C>A
ENST00000355622.6:c.1097C>A	ENSP00000363089.5:p.Ala366Asp
ENST00000394487.4:c.977C>A	ENSP00000377997.4:p.Ala326Asp
ENST00000472304.1:n.1014C>A
NM_003266.3:c.977C>A	NP_003257.1:p.Ala326Asp
NM_138554.4:c.1097C>A	NP_612564.1:p.Ala366Asp
NM_138557.2:c.497C>A	NP_612567.1:p.Ala166Asp
NM_138554.5:c.1097C>A MANE Select	NP_612564.1:p.Ala366Asp
NM_003266.4:c.977C>A	NP_003257.1:p.Ala326Asp
NM_138557.3:c.497C>A	NP_612567.1:p.Ala166Asp