Canonical Allele Identifier: CA1875361541
Gene: TLR4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.117710186_117710190delinsATAGT , CM000671.2:g.117710186_117710190delinsATAGT GRCh38
NC_000009.11:g.120472464_120472468delinsATAGT , CM000671.1:g.120472464_120472468delinsATAGT GRCh37
NC_000009.10:g.119512285_119512289delinsATAGT NCBI36
NG_011475.1:g.11005_11009delinsATAGT
NG_011475.2:g.10784_10788delinsATAGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000646089.2:c.93+5621_93+5625delinsATAGT ENSP00000496197.1:n.93+5621_93+5625delinsATAGT
ENST00000697624.1:n.200+5621_200+5625delinsATAGT
ENST00000697625.1:c.93+5621_93+5625delinsATAGT ENSP00000513362.1:n.93+5621_93+5625delinsATAGT
ENST00000697636.1:c.93+5621_93+5625delinsATAGT ENSP00000513366.1:n.93+5621_93+5625delinsATAGT
ENST00000697637.1:c.93+5621_93+5625delinsATAGT ENSP00000513367.1:n.93+5621_93+5625delinsATAGT
ENST00000697664.1:c.140+1457_140+1461delinsATAGT ENSP00000513389.1:n.140+1457_140+1461delinsATAGT
ENST00000697665.1:c.93+5621_93+5625delinsATAGT ENSP00000513390.1:n.93+5621_93+5625delinsATAGT
ENST00000697666.1:c.140+1457_140+1461delinsATAGT ENSP00000513391.1:n.140+1457_140+1461delinsATAGT
ENST00000355622.8:c.260+1457_260+1461delinsATAGT MANE Select ENSP00000363089.5:n.260+1457_260+1461delinsATAGT
ENST00000394487.5:c.140+1457_140+1461delinsATAGT ENSP00000377997.4:n.140+1457_140+1461delinsATAGT
ENST00000472304.2:c.94-2203_94-2199delinsATAGT ENSP00000496429.1:n.94-2203_94-2199delinsATAGT
ENST00000642985.1:c.260+1457_260+1461delinsATAGT ENSP00000493686.1:n.260+1457_260+1461delinsATAGT
ENST00000646089.1:c.93+5621_93+5625delinsATAGT ENSP00000496197.1:n.93+5621_93+5625delinsATAGT
ENST00000665764.1:c.93+5621_93+5625delinsATAGT ENSP00000499745.1:n.93+5621_93+5625delinsATAGT
ENST00000355622.6:c.260+1457_260+1461delinsATAGT ENSP00000363089.5:n.260+1457_260+1461delinsATAGT
ENST00000394487.4:c.140+1457_140+1461delinsATAGT ENSP00000377997.4:n.140+1457_140+1461delinsATAGT
ENST00000472304.1:n.178-2203_178-2199delinsATAGT
NM_003266.3:c.140+1457_140+1461delinsATAGT NP_003257.1:n.140+1457_140+1461delinsATAGT
NM_138554.4:c.260+1457_260+1461delinsATAGT NP_612564.1:n.260+1457_260+1461delinsATAGT
NM_138557.2:c.-340-2203_-340-2199delinsATAGT NP_612567.1:n.-340-2203_-340-2199delinsATAGT
NM_138554.5:c.260+1457_260+1461delinsATAGT MANE Select NP_612564.1:n.260+1457_260+1461delinsATAGT
NM_003266.4:c.140+1457_140+1461delinsATAGT NP_003257.1:n.140+1457_140+1461delinsATAGT
NM_138557.3:c.-340-2203_-340-2199delinsATAGT NP_612567.1:n.-340-2203_-340-2199delinsATAGT