Canonical Allele Identifier: CA374659307
Gene: TLR4 HGNC NCBI

Linked Data

dbSNP Id: rs13294155

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.117717785G>C , CM000671.2:g.117717785G>C GRCh38
NC_000009.11:g.120480063G>C , CM000671.1:g.120480063G>C GRCh37
NC_000009.10:g.119519884G>C NCBI36
NG_011475.1:g.18604G>C
NG_011475.2:g.18383G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000646089.2:c.93+13220G>C ENSP00000496197.1:n.93+13220G>C
ENST00000697624.1:n.200+13220G>C
ENST00000697625.1:c.93+13220G>C ENSP00000513362.1:n.93+13220G>C
ENST00000697636.1:c.93+13220G>C ENSP00000513366.1:n.93+13220G>C
ENST00000697637.1:c.93+13220G>C ENSP00000513367.1:n.93+13220G>C
ENST00000697664.1:c.140+9056G>C ENSP00000513389.1:n.140+9056G>C
ENST00000697665.1:c.93+13220G>C ENSP00000513390.1:n.93+13220G>C
ENST00000697666.1:c.140+9056G>C ENSP00000513391.1:n.140+9056G>C
ENST00000355622.8:c.*3137G>C MANE Select ENSP00000363089.5:n.*3137G>C
ENST00000642985.1:c.260+9056G>C ENSP00000493686.1:n.260+9056G>C
ENST00000646089.1:c.93+13220G>C ENSP00000496197.1:n.93+13220G>C
ENST00000665764.1:c.93+13220G>C ENSP00000499745.1:n.93+13220G>C
NM_138554.5:c.*3137G>C MANE Select NP_612564.1:n.*3137G>C
NM_003266.4:c.*3137G>C NP_003257.1:n.*3137G>C
NM_138557.3:c.*3137G>C NP_612567.1:n.*3137G>C