Canonical Allele Identifier: CA1875362715

Gene: TLR4

Linked Data

• dbSNP Id: rs1829414740

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.117720844C>G , CM000671.2:g.117720844C>G	GRCh38
NC_000009.11:g.120483122C>G , CM000671.1:g.120483122C>G	GRCh37
NC_000009.10:g.119522943C>G	NCBI36
NG_011475.2:g.21442C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000646089.2:c.93+16279C>G	ENSP00000496197.1:n.93+16279C>G
ENST00000697624.1:n.200+16279C>G
ENST00000697625.1:c.93+16279C>G	ENSP00000513362.1:n.93+16279C>G
ENST00000697636.1:c.93+16279C>G	ENSP00000513366.1:n.93+16279C>G
ENST00000697637.1:c.93+16279C>G	ENSP00000513367.1:n.93+16279C>G
ENST00000697664.1:c.140+12115C>G	ENSP00000513389.1:n.140+12115C>G
ENST00000697665.1:c.93+16279C>G	ENSP00000513390.1:n.93+16279C>G
ENST00000697666.1:c.140+12115C>G	ENSP00000513391.1:n.140+12115C>G
ENST00000355622.8:c.*6196C>G MANE Select	ENSP00000363089.5:n.*6196C>G
ENST00000642985.1:c.260+12115C>G	ENSP00000493686.1:n.260+12115C>G
ENST00000646089.1:c.93+16279C>G	ENSP00000496197.1:n.93+16279C>G
ENST00000665764.1:c.93+16279C>G	ENSP00000499745.1:n.93+16279C>G
NM_138554.5:c.*6196C>G MANE Select	NP_612564.1:n.*6196C>G
NM_003266.4:c.*6196C>G	NP_003257.1:n.*6196C>G
NM_138557.3:c.*6196C>G	NP_612567.1:n.*6196C>G