Canonical Allele Identifier: CA1875354641

Gene: TLR4

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.117713634_117713638delinsCCTCT , CM000671.2:g.117713634_117713638delinsCCTCT	GRCh38
NC_000009.11:g.120475912_120475916delinsCCTCT , CM000671.1:g.120475912_120475916delinsCCTCT	GRCh37
NC_000009.10:g.119515733_119515737delinsCCTCT	NCBI36
NG_011475.1:g.14453_14457delinsCCTCT
NG_011475.2:g.14232_14236delinsCCTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646089.2:c.93+9069_93+9073delinsCCTCT	ENSP00000496197.1:n.93+9069_93+9073delinsCCTCT
ENST00000697624.1:n.200+9069_200+9073delinsCCTCT
ENST00000697625.1:c.93+9069_93+9073delinsCCTCT	ENSP00000513362.1:n.93+9069_93+9073delinsCCTCT
ENST00000697636.1:c.93+9069_93+9073delinsCCTCT	ENSP00000513366.1:n.93+9069_93+9073delinsCCTCT
ENST00000697637.1:c.93+9069_93+9073delinsCCTCT	ENSP00000513367.1:n.93+9069_93+9073delinsCCTCT
ENST00000697664.1:c.140+4905_140+4909delinsCCTCT	ENSP00000513389.1:n.140+4905_140+4909delinsCCTCT
ENST00000697665.1:c.93+9069_93+9073delinsCCTCT	ENSP00000513390.1:n.93+9069_93+9073delinsCCTCT
ENST00000697666.1:c.140+4905_140+4909delinsCCTCT	ENSP00000513391.1:n.140+4905_140+4909delinsCCTCT
ENST00000355622.8:c.1506_1510delinsCCTCT MANE Select	ENSP00000363089.5:p.Asp502=
ENST00000394487.5:c.1386_1390delinsCCTCT	ENSP00000377997.4:p.Asp462=
ENST00000472304.2:c.*1240_*1244delinsCCTCT	ENSP00000496429.1:n.*1240_*1244delinsCCTCT
ENST00000642985.1:c.260+4905_260+4909delinsCCTCT	ENSP00000493686.1:n.260+4905_260+4909delinsCCTCT
ENST00000646089.1:c.93+9069_93+9073delinsCCTCT	ENSP00000496197.1:n.93+9069_93+9073delinsCCTCT
ENST00000665764.1:c.93+9069_93+9073delinsCCTCT	ENSP00000499745.1:n.93+9069_93+9073delinsCCTCT
ENST00000355622.6:c.1506_1510delinsCCTCT	ENSP00000363089.5:p.Asp502=
ENST00000394487.4:c.1386_1390delinsCCTCT	ENSP00000377997.4:p.Asp462=
ENST00000472304.1:n.1423_1427delinsCCTCT
NM_003266.3:c.1386_1390delinsCCTCT	NP_003257.1:p.Asp462=
NM_138554.4:c.1506_1510delinsCCTCT	NP_612564.1:p.Asp502=
NM_138557.2:c.906_910delinsCCTCT	NP_612567.1:p.Asp302=
NM_138554.5:c.1506_1510delinsCCTCT MANE Select	NP_612564.1:p.Asp502=
NM_003266.4:c.1386_1390delinsCCTCT	NP_003257.1:p.Asp462=
NM_138557.3:c.906_910delinsCCTCT	NP_612567.1:p.Asp302=