Canonical Allele Identifier: CA2840541241
Gene: TLR4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.117721713A>T , CM000671.2:g.117721713A>T GRCh38
NC_000009.11:g.120483991A>T , CM000671.1:g.120483991A>T GRCh37
NC_000009.10:g.119523812A>T NCBI36
NG_011475.2:g.22311A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000646089.2:c.93+17148A>T ENSP00000496197.1:n.93+17148A>T
ENST00000697624.1:n.200+17148A>T
ENST00000697625.1:c.93+17148A>T ENSP00000513362.1:n.93+17148A>T
ENST00000697636.1:c.93+17148A>T ENSP00000513366.1:n.93+17148A>T
ENST00000697637.1:c.93+17148A>T ENSP00000513367.1:n.93+17148A>T
ENST00000697664.1:c.140+12984A>T ENSP00000513389.1:n.140+12984A>T
ENST00000697665.1:c.93+17148A>T ENSP00000513390.1:n.93+17148A>T
ENST00000697666.1:c.140+12984A>T ENSP00000513391.1:n.140+12984A>T
ENST00000355622.8:c.*7065A>T MANE Select ENSP00000363089.5:n.*7065A>T
ENST00000642985.1:c.260+12984A>T ENSP00000493686.1:n.260+12984A>T
ENST00000646089.1:c.93+17148A>T ENSP00000496197.1:n.93+17148A>T
ENST00000665764.1:c.93+17148A>T ENSP00000499745.1:n.93+17148A>T
NM_138554.5:c.*7065A>T MANE Select NP_612564.1:n.*7065A>T
NM_003266.4:c.*7065A>T NP_003257.1:n.*7065A>T
NM_138557.3:c.*7065A>T NP_612567.1:n.*7065A>T