Canonical Allele Identifier: CA1875354603

Gene: TLR4

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.117713592_117713594delinsTCC , CM000671.2:g.117713592_117713594delinsTCC	GRCh38
NC_000009.11:g.120475870_120475872delinsTCC , CM000671.1:g.120475870_120475872delinsTCC	GRCh37
NC_000009.10:g.119515691_119515693delinsTCC	NCBI36
NG_011475.1:g.14411_14413delinsTCC
NG_011475.2:g.14190_14192delinsTCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646089.2:c.93+9027_93+9029delinsTCC	ENSP00000496197.1:n.93+9027_93+9029delinsTCC
ENST00000697624.1:n.200+9027_200+9029delinsTCC
ENST00000697625.1:c.93+9027_93+9029delinsTCC	ENSP00000513362.1:n.93+9027_93+9029delinsTCC
ENST00000697636.1:c.93+9027_93+9029delinsTCC	ENSP00000513366.1:n.93+9027_93+9029delinsTCC
ENST00000697637.1:c.93+9027_93+9029delinsTCC	ENSP00000513367.1:n.93+9027_93+9029delinsTCC
ENST00000697664.1:c.140+4863_140+4865delinsTCC	ENSP00000513389.1:n.140+4863_140+4865delinsTCC
ENST00000697665.1:c.93+9027_93+9029delinsTCC	ENSP00000513390.1:n.93+9027_93+9029delinsTCC
ENST00000697666.1:c.140+4863_140+4865delinsTCC	ENSP00000513391.1:n.140+4863_140+4865delinsTCC
ENST00000355622.8:c.1464_1466delinsTCC MANE Select	ENSP00000363089.5:p.Leu488=
ENST00000394487.5:c.1344_1346delinsTCC	ENSP00000377997.4:p.Leu448=
ENST00000472304.2:c.*1198_*1200delinsTCC	ENSP00000496429.1:n.*1198_*1200delinsTCC
ENST00000642985.1:c.260+4863_260+4865delinsTCC	ENSP00000493686.1:n.260+4863_260+4865delinsTCC
ENST00000646089.1:c.93+9027_93+9029delinsTCC	ENSP00000496197.1:n.93+9027_93+9029delinsTCC
ENST00000665764.1:c.93+9027_93+9029delinsTCC	ENSP00000499745.1:n.93+9027_93+9029delinsTCC
ENST00000355622.6:c.1464_1466delinsTCC	ENSP00000363089.5:p.Leu488=
ENST00000394487.4:c.1344_1346delinsTCC	ENSP00000377997.4:p.Leu448=
ENST00000472304.1:n.1381_1383delinsTCC
NM_003266.3:c.1344_1346delinsTCC	NP_003257.1:p.Leu448=
NM_138554.4:c.1464_1466delinsTCC	NP_612564.1:p.Leu488=
NM_138557.2:c.864_866delinsTCC	NP_612567.1:p.Leu288=
NM_138554.5:c.1464_1466delinsTCC MANE Select	NP_612564.1:p.Leu488=
NM_003266.4:c.1344_1346delinsTCC	NP_003257.1:p.Leu448=
NM_138557.3:c.864_866delinsTCC	NP_612567.1:p.Leu288=