Canonical Allele Identifier: CA1128556257
Gene: TLR4 HGNC NCBI

Linked Data

dbSNP Id: rs1829424844

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.117721740_117721743del , CM000671.2:g.117721740_117721743del GRCh38
NC_000009.11:g.120484018_120484021del , CM000671.1:g.120484018_120484021del GRCh37
NC_000009.10:g.119523839_119523842del NCBI36
NG_011475.2:g.22338_22341del

Transcript Alleles

HGVS Amino-acid Change
ENST00000646089.2:c.93+17175_93+17178del ENSP00000496197.1:n.93+17175_93+17178del
ENST00000697624.1:n.200+17175_200+17178del
ENST00000697625.1:c.93+17175_93+17178del ENSP00000513362.1:n.93+17175_93+17178del
ENST00000697636.1:c.93+17175_93+17178del ENSP00000513366.1:n.93+17175_93+17178del
ENST00000697637.1:c.93+17175_93+17178del ENSP00000513367.1:n.93+17175_93+17178del
ENST00000697664.1:c.140+13011_140+13014del ENSP00000513389.1:n.140+13011_140+13014del
ENST00000697665.1:c.93+17175_93+17178del ENSP00000513390.1:n.93+17175_93+17178del
ENST00000697666.1:c.140+13011_140+13014del ENSP00000513391.1:n.140+13011_140+13014del
ENST00000355622.8:c.*7092_*7095del MANE Select ENSP00000363089.5:n.*7092_*7095del
ENST00000642985.1:c.260+13011_260+13014del ENSP00000493686.1:n.260+13011_260+13014del
ENST00000646089.1:c.93+17175_93+17178del ENSP00000496197.1:n.93+17175_93+17178del
ENST00000665764.1:c.93+17175_93+17178del ENSP00000499745.1:n.93+17175_93+17178del
NM_138554.5:c.*7092_*7095del MANE Select NP_612564.1:n.*7092_*7095del
NM_003266.4:c.*7092_*7095del NP_003257.1:n.*7092_*7095del
NM_138557.3:c.*7092_*7095del NP_612567.1:n.*7092_*7095del