Canonical Allele Identifier: CA1875354724
Gene: TLR4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.117713668A= , CM000671.2:g.117713668A= GRCh38
NC_000009.11:g.120475946A= , CM000671.1:g.120475946A= GRCh37
NC_000009.10:g.119515767A= NCBI36
NG_011475.1:g.14487A=
NG_011475.2:g.14266A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000646089.2:c.93+9103A= ENSP00000496197.1:n.93+9103A=
ENST00000697624.1:n.200+9103A=
ENST00000697625.1:c.93+9103A= ENSP00000513362.1:n.93+9103A=
ENST00000697636.1:c.93+9103A= ENSP00000513366.1:n.93+9103A=
ENST00000697637.1:c.93+9103A= ENSP00000513367.1:n.93+9103A=
ENST00000697664.1:c.140+4939A= ENSP00000513389.1:n.140+4939A=
ENST00000697665.1:c.93+9103A= ENSP00000513390.1:n.93+9103A=
ENST00000697666.1:c.140+4939A= ENSP00000513391.1:n.140+4939A=
ENST00000355622.8:c.1540A= MANE Select ENSP00000363089.5:p.Thr514=
ENST00000394487.5:c.1420A= ENSP00000377997.4:p.Thr474=
ENST00000472304.2:c.*1274A= ENSP00000496429.1:n.*1274A=
ENST00000642985.1:c.260+4939A= ENSP00000493686.1:n.260+4939A=
ENST00000646089.1:c.93+9103A= ENSP00000496197.1:n.93+9103A=
ENST00000665764.1:c.93+9103A= ENSP00000499745.1:n.93+9103A=
ENST00000355622.6:c.1540A= ENSP00000363089.5:p.Thr514=
ENST00000394487.4:c.1420A= ENSP00000377997.4:p.Thr474=
ENST00000472304.1:n.1457A=
NM_003266.3:c.1420A= NP_003257.1:p.Thr474=
NM_138554.4:c.1540A= NP_612564.1:p.Thr514=
NM_138557.2:c.940A= NP_612567.1:p.Thr314=
NM_138554.5:c.1540A= MANE Select NP_612564.1:p.Thr514=
NM_003266.4:c.1420A= NP_003257.1:p.Thr474=
NM_138557.3:c.940A= NP_612567.1:p.Thr314=