Canonical Allele Identifier: CA374656530
Gene: TLR4 HGNC NCBI

Linked Data

dbSNP Id: rs1462969834

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.117713401G>A , CM000671.2:g.117713401G>A GRCh38
NC_000009.11:g.120475679G>A , CM000671.1:g.120475679G>A GRCh37
NC_000009.10:g.119515500G>A NCBI36
NG_011475.1:g.14220G>A
NG_011475.2:g.13999G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000646089.2:c.93+8836G>A ENSP00000496197.1:n.93+8836G>A
ENST00000697624.1:n.200+8836G>A
ENST00000697625.1:c.93+8836G>A ENSP00000513362.1:n.93+8836G>A
ENST00000697636.1:c.93+8836G>A ENSP00000513366.1:n.93+8836G>A
ENST00000697637.1:c.93+8836G>A ENSP00000513367.1:n.93+8836G>A
ENST00000697664.1:c.140+4672G>A ENSP00000513389.1:n.140+4672G>A
ENST00000697665.1:c.93+8836G>A ENSP00000513390.1:n.93+8836G>A
ENST00000697666.1:c.140+4672G>A ENSP00000513391.1:n.140+4672G>A
ENST00000355622.8:c.1273G>A MANE Select ENSP00000363089.5:p.Glu425Lys
ENST00000394487.5:c.1153G>A ENSP00000377997.4:p.Glu385Lys
ENST00000472304.2:c.*1007G>A ENSP00000496429.1:n.*1007G>A
ENST00000642985.1:c.260+4672G>A ENSP00000493686.1:n.260+4672G>A
ENST00000646089.1:c.93+8836G>A ENSP00000496197.1:n.93+8836G>A
ENST00000665764.1:c.93+8836G>A ENSP00000499745.1:n.93+8836G>A
ENST00000355622.6:c.1273G>A ENSP00000363089.5:p.Glu425Lys
ENST00000394487.4:c.1153G>A ENSP00000377997.4:p.Glu385Lys
ENST00000472304.1:n.1190G>A
NM_003266.3:c.1153G>A NP_003257.1:p.Glu385Lys
NM_138554.4:c.1273G>A NP_612564.1:p.Glu425Lys
NM_138557.2:c.673G>A NP_612567.1:p.Glu225Lys
NM_138554.5:c.1273G>A MANE Select NP_612564.1:p.Glu425Lys
NM_003266.4:c.1153G>A NP_003257.1:p.Glu385Lys
NM_138557.3:c.673G>A NP_612567.1:p.Glu225Lys