Canonical Allele Identifier: CA1875360938
Gene: TLR4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.117718049_117718051delinsCAT , CM000671.2:g.117718049_117718051delinsCAT GRCh38
NC_000009.11:g.120480327_120480329delinsCAT , CM000671.1:g.120480327_120480329delinsCAT GRCh37
NC_000009.10:g.119520148_119520150delinsCAT NCBI36
NG_011475.1:g.18868_18870delinsCAT
NG_011475.2:g.18647_18649delinsCAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000646089.2:c.93+13484_93+13486delinsCAT ENSP00000496197.1:n.93+13484_93+13486delinsCAT
ENST00000697624.1:n.200+13484_200+13486delinsCAT
ENST00000697625.1:c.93+13484_93+13486delinsCAT ENSP00000513362.1:n.93+13484_93+13486delinsCAT
ENST00000697636.1:c.93+13484_93+13486delinsCAT ENSP00000513366.1:n.93+13484_93+13486delinsCAT
ENST00000697637.1:c.93+13484_93+13486delinsCAT ENSP00000513367.1:n.93+13484_93+13486delinsCAT
ENST00000697664.1:c.140+9320_140+9322delinsCAT ENSP00000513389.1:n.140+9320_140+9322delinsCAT
ENST00000697665.1:c.93+13484_93+13486delinsCAT ENSP00000513390.1:n.93+13484_93+13486delinsCAT
ENST00000697666.1:c.140+9320_140+9322delinsCAT ENSP00000513391.1:n.140+9320_140+9322delinsCAT
ENST00000355622.8:c.*3401_*3403delinsCAT MANE Select ENSP00000363089.5:n.*3401_*3403delinsCAT
ENST00000642985.1:c.260+9320_260+9322delinsCAT ENSP00000493686.1:n.260+9320_260+9322delinsCAT
ENST00000646089.1:c.93+13484_93+13486delinsCAT ENSP00000496197.1:n.93+13484_93+13486delinsCAT
ENST00000665764.1:c.93+13484_93+13486delinsCAT ENSP00000499745.1:n.93+13484_93+13486delinsCAT
NM_138554.5:c.*3401_*3403delinsCAT MANE Select NP_612564.1:n.*3401_*3403delinsCAT
NM_003266.4:c.*3401_*3403delinsCAT NP_003257.1:n.*3401_*3403delinsCAT
NM_138557.3:c.*3401_*3403delinsCAT NP_612567.1:n.*3401_*3403delinsCAT