Canonical Allele Identifier: CA1875354763
Gene: TLR4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.117713689_117713690delinsAG , CM000671.2:g.117713689_117713690delinsAG GRCh38
NC_000009.11:g.120475967_120475968delinsAG , CM000671.1:g.120475967_120475968delinsAG GRCh37
NC_000009.10:g.119515788_119515789delinsAG NCBI36
NG_011475.1:g.14508_14509delinsAG
NG_011475.2:g.14287_14288delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000646089.2:c.93+9124_93+9125delinsAG ENSP00000496197.1:n.93+9124_93+9125delinsAG
ENST00000697624.1:n.200+9124_200+9125delinsAG
ENST00000697625.1:c.93+9124_93+9125delinsAG ENSP00000513362.1:n.93+9124_93+9125delinsAG
ENST00000697636.1:c.93+9124_93+9125delinsAG ENSP00000513366.1:n.93+9124_93+9125delinsAG
ENST00000697637.1:c.93+9124_93+9125delinsAG ENSP00000513367.1:n.93+9124_93+9125delinsAG
ENST00000697664.1:c.140+4960_140+4961delinsAG ENSP00000513389.1:n.140+4960_140+4961delinsAG
ENST00000697665.1:c.93+9124_93+9125delinsAG ENSP00000513390.1:n.93+9124_93+9125delinsAG
ENST00000697666.1:c.140+4960_140+4961delinsAG ENSP00000513391.1:n.140+4960_140+4961delinsAG
ENST00000355622.8:c.1561_1562delinsAG MANE Select ENSP00000363089.5:p.Ser521=
ENST00000394487.5:c.1441_1442delinsAG ENSP00000377997.4:p.Ser481=
ENST00000472304.2:c.*1295_*1296delinsAG ENSP00000496429.1:n.*1295_*1296delinsAG
ENST00000642985.1:c.260+4960_260+4961delinsAG ENSP00000493686.1:n.260+4960_260+4961delinsAG
ENST00000646089.1:c.93+9124_93+9125delinsAG ENSP00000496197.1:n.93+9124_93+9125delinsAG
ENST00000665764.1:c.93+9124_93+9125delinsAG ENSP00000499745.1:n.93+9124_93+9125delinsAG
ENST00000355622.6:c.1561_1562delinsAG ENSP00000363089.5:p.Ser521=
ENST00000394487.4:c.1441_1442delinsAG ENSP00000377997.4:p.Ser481=
ENST00000472304.1:n.1478_1479delinsAG
NM_003266.3:c.1441_1442delinsAG NP_003257.1:p.Ser481=
NM_138554.4:c.1561_1562delinsAG NP_612564.1:p.Ser521=
NM_138557.2:c.961_962delinsAG NP_612567.1:p.Ser321=
NM_138554.5:c.1561_1562delinsAG MANE Select NP_612564.1:p.Ser521=
NM_003266.4:c.1441_1442delinsAG NP_003257.1:p.Ser481=
NM_138557.3:c.961_962delinsAG NP_612567.1:p.Ser321=