Canonical Allele Identifier: CA1875363059
Gene: TLR4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.117721610_117721616delinsATGTGTC , CM000671.2:g.117721610_117721616delinsATGTGTC GRCh38
NC_000009.11:g.120483888_120483894delinsATGTGTC , CM000671.1:g.120483888_120483894delinsATGTGTC GRCh37
NC_000009.10:g.119523709_119523715delinsATGTGTC NCBI36
NG_011475.2:g.22208_22214delinsATGTGTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000646089.2:c.93+17045_93+17051delinsATGTGTC ENSP00000496197.1:n.93+17045_93+17051delinsATGTGTC
ENST00000697624.1:n.200+17045_200+17051delinsATGTGTC
ENST00000697625.1:c.93+17045_93+17051delinsATGTGTC ENSP00000513362.1:n.93+17045_93+17051delinsATGTGTC
ENST00000697636.1:c.93+17045_93+17051delinsATGTGTC ENSP00000513366.1:n.93+17045_93+17051delinsATGTGTC
ENST00000697637.1:c.93+17045_93+17051delinsATGTGTC ENSP00000513367.1:n.93+17045_93+17051delinsATGTGTC
ENST00000697664.1:c.140+12881_140+12887delinsATGTGTC ENSP00000513389.1:n.140+12881_140+12887delinsATGTGTC
ENST00000697665.1:c.93+17045_93+17051delinsATGTGTC ENSP00000513390.1:n.93+17045_93+17051delinsATGTGTC
ENST00000697666.1:c.140+12881_140+12887delinsATGTGTC ENSP00000513391.1:n.140+12881_140+12887delinsATGTGTC
ENST00000355622.8:c.*6962_*6968delinsATGTGTC MANE Select ENSP00000363089.5:n.*6962_*6968delinsATGTGTC
ENST00000642985.1:c.260+12881_260+12887delinsATGTGTC ENSP00000493686.1:n.260+12881_260+12887delinsATGTGTC
ENST00000646089.1:c.93+17045_93+17051delinsATGTGTC ENSP00000496197.1:n.93+17045_93+17051delinsATGTGTC
ENST00000665764.1:c.93+17045_93+17051delinsATGTGTC ENSP00000499745.1:n.93+17045_93+17051delinsATGTGTC
NM_138554.5:c.*6962_*6968delinsATGTGTC MANE Select NP_612564.1:n.*6962_*6968delinsATGTGTC
NM_003266.4:c.*6962_*6968delinsATGTGTC NP_003257.1:n.*6962_*6968delinsATGTGTC
NM_138557.3:c.*6962_*6968delinsATGTGTC NP_612567.1:n.*6962_*6968delinsATGTGTC