Canonical Allele Identifier: CA1875361443
Gene: TLR4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.117718501_117718504delinsAGAG , CM000671.2:g.117718501_117718504delinsAGAG GRCh38
NC_000009.11:g.120480779_120480782delinsAGAG , CM000671.1:g.120480779_120480782delinsAGAG GRCh37
NC_000009.10:g.119520600_119520603delinsAGAG NCBI36
NG_011475.1:g.19320_19323delinsAGAG
NG_011475.2:g.19099_19102delinsAGAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000646089.2:c.93+13936_93+13939delinsAGAG ENSP00000496197.1:n.93+13936_93+13939delinsAGAG
ENST00000697624.1:n.200+13936_200+13939delinsAGAG
ENST00000697625.1:c.93+13936_93+13939delinsAGAG ENSP00000513362.1:n.93+13936_93+13939delinsAGAG
ENST00000697636.1:c.93+13936_93+13939delinsAGAG ENSP00000513366.1:n.93+13936_93+13939delinsAGAG
ENST00000697637.1:c.93+13936_93+13939delinsAGAG ENSP00000513367.1:n.93+13936_93+13939delinsAGAG
ENST00000697664.1:c.140+9772_140+9775delinsAGAG ENSP00000513389.1:n.140+9772_140+9775delinsAGAG
ENST00000697665.1:c.93+13936_93+13939delinsAGAG ENSP00000513390.1:n.93+13936_93+13939delinsAGAG
ENST00000697666.1:c.140+9772_140+9775delinsAGAG ENSP00000513391.1:n.140+9772_140+9775delinsAGAG
ENST00000355622.8:c.*3853_*3856delinsAGAG MANE Select ENSP00000363089.5:n.*3853_*3856delinsAGAG
ENST00000642985.1:c.260+9772_260+9775delinsAGAG ENSP00000493686.1:n.260+9772_260+9775delinsAGAG
ENST00000646089.1:c.93+13936_93+13939delinsAGAG ENSP00000496197.1:n.93+13936_93+13939delinsAGAG
ENST00000665764.1:c.93+13936_93+13939delinsAGAG ENSP00000499745.1:n.93+13936_93+13939delinsAGAG
NM_138554.5:c.*3853_*3856delinsAGAG MANE Select NP_612564.1:n.*3853_*3856delinsAGAG
NM_003266.4:c.*3853_*3856delinsAGAG NP_003257.1:n.*3853_*3856delinsAGAG
NM_138557.3:c.*3853_*3856delinsAGAG NP_612567.1:n.*3853_*3856delinsAGAG