Canonical Allele Identifier: CA1875354922
Gene: TLR4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.117713792A= , CM000671.2:g.117713792A= GRCh38
NC_000009.11:g.120476070A= , CM000671.1:g.120476070A= GRCh37
NC_000009.10:g.119515891A= NCBI36
NG_011475.1:g.14611A=
NG_011475.2:g.14390A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000646089.2:c.93+9227A= ENSP00000496197.1:n.93+9227A=
ENST00000697624.1:n.200+9227A=
ENST00000697625.1:c.93+9227A= ENSP00000513362.1:n.93+9227A=
ENST00000697636.1:c.93+9227A= ENSP00000513366.1:n.93+9227A=
ENST00000697637.1:c.93+9227A= ENSP00000513367.1:n.93+9227A=
ENST00000697664.1:c.140+5063A= ENSP00000513389.1:n.140+5063A=
ENST00000697665.1:c.93+9227A= ENSP00000513390.1:n.93+9227A=
ENST00000697666.1:c.140+5063A= ENSP00000513391.1:n.140+5063A=
ENST00000355622.8:c.1664A= MANE Select ENSP00000363089.5:p.His555=
ENST00000394487.5:c.1544A= ENSP00000377997.4:p.His515=
ENST00000472304.2:c.*1398A= ENSP00000496429.1:n.*1398A=
ENST00000642985.1:c.260+5063A= ENSP00000493686.1:n.260+5063A=
ENST00000646089.1:c.93+9227A= ENSP00000496197.1:n.93+9227A=
ENST00000665764.1:c.93+9227A= ENSP00000499745.1:n.93+9227A=
ENST00000355622.6:c.1664A= ENSP00000363089.5:p.His555=
ENST00000394487.4:c.1544A= ENSP00000377997.4:p.His515=
ENST00000472304.1:n.1581A=
NM_003266.3:c.1544A= NP_003257.1:p.His515=
NM_138554.4:c.1664A= NP_612564.1:p.His555=
NM_138557.2:c.1064A= NP_612567.1:p.His355=
NM_138554.5:c.1664A= MANE Select NP_612564.1:p.His555=
NM_003266.4:c.1544A= NP_003257.1:p.His515=
NM_138557.3:c.1064A= NP_612567.1:p.His355=