Canonical Allele Identifier: CA1875361455
Gene: TLR4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.117710077_117710082delinsATAATT , CM000671.2:g.117710077_117710082delinsATAATT GRCh38
NC_000009.11:g.120472355_120472360delinsATAATT , CM000671.1:g.120472355_120472360delinsATAATT GRCh37
NC_000009.10:g.119512176_119512181delinsATAATT NCBI36
NG_011475.1:g.10896_10901delinsATAATT
NG_011475.2:g.10675_10680delinsATAATT

Transcript Alleles

HGVS Amino-acid Change
ENST00000646089.2:c.93+5512_93+5517delinsATAATT ENSP00000496197.1:n.93+5512_93+5517delinsATAATT
ENST00000697624.1:n.200+5512_200+5517delinsATAATT
ENST00000697625.1:c.93+5512_93+5517delinsATAATT ENSP00000513362.1:n.93+5512_93+5517delinsATAATT
ENST00000697636.1:c.93+5512_93+5517delinsATAATT ENSP00000513366.1:n.93+5512_93+5517delinsATAATT
ENST00000697637.1:c.93+5512_93+5517delinsATAATT ENSP00000513367.1:n.93+5512_93+5517delinsATAATT
ENST00000697664.1:c.140+1348_140+1353delinsATAATT ENSP00000513389.1:n.140+1348_140+1353delinsATAATT
ENST00000697665.1:c.93+5512_93+5517delinsATAATT ENSP00000513390.1:n.93+5512_93+5517delinsATAATT
ENST00000697666.1:c.140+1348_140+1353delinsATAATT ENSP00000513391.1:n.140+1348_140+1353delinsATAATT
ENST00000355622.8:c.260+1348_260+1353delinsATAATT MANE Select ENSP00000363089.5:n.260+1348_260+1353delinsATAATT
ENST00000394487.5:c.140+1348_140+1353delinsATAATT ENSP00000377997.4:n.140+1348_140+1353delinsATAATT
ENST00000472304.2:c.94-2312_94-2307delinsATAATT ENSP00000496429.1:n.94-2312_94-2307delinsATAATT
ENST00000642985.1:c.260+1348_260+1353delinsATAATT ENSP00000493686.1:n.260+1348_260+1353delinsATAATT
ENST00000646089.1:c.93+5512_93+5517delinsATAATT ENSP00000496197.1:n.93+5512_93+5517delinsATAATT
ENST00000665764.1:c.93+5512_93+5517delinsATAATT ENSP00000499745.1:n.93+5512_93+5517delinsATAATT
ENST00000355622.6:c.260+1348_260+1353delinsATAATT ENSP00000363089.5:n.260+1348_260+1353delinsATAATT
ENST00000394487.4:c.140+1348_140+1353delinsATAATT ENSP00000377997.4:n.140+1348_140+1353delinsATAATT
ENST00000472304.1:n.178-2312_178-2307delinsATAATT
NM_003266.3:c.140+1348_140+1353delinsATAATT NP_003257.1:n.140+1348_140+1353delinsATAATT
NM_138554.4:c.260+1348_260+1353delinsATAATT NP_612564.1:n.260+1348_260+1353delinsATAATT
NM_138557.2:c.-340-2312_-340-2307delinsATAATT NP_612567.1:n.-340-2312_-340-2307delinsATAATT
NM_138554.5:c.260+1348_260+1353delinsATAATT MANE Select NP_612564.1:n.260+1348_260+1353delinsATAATT
NM_003266.4:c.140+1348_140+1353delinsATAATT NP_003257.1:n.140+1348_140+1353delinsATAATT
NM_138557.3:c.-340-2312_-340-2307delinsATAATT NP_612567.1:n.-340-2312_-340-2307delinsATAATT