Canonical Allele Identifier: CA1875354928

Gene: TLR4

Linked Data

• dbSNP Id: rs1829287978

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.117713797_117713802del , CM000671.2:g.117713797_117713802del	GRCh38
NC_000009.11:g.120476075_120476080del , CM000671.1:g.120476075_120476080del	GRCh37
NC_000009.10:g.119515896_119515901del	NCBI36
NG_011475.1:g.14616_14621del
NG_011475.2:g.14395_14400del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646089.2:c.93+9232_93+9237del	ENSP00000496197.1:n.93+9232_93+9237del
ENST00000697624.1:n.200+9232_200+9237del
ENST00000697625.1:c.93+9232_93+9237del	ENSP00000513362.1:n.93+9232_93+9237del
ENST00000697636.1:c.93+9232_93+9237del	ENSP00000513366.1:n.93+9232_93+9237del
ENST00000697637.1:c.93+9232_93+9237del	ENSP00000513367.1:n.93+9232_93+9237del
ENST00000697664.1:c.140+5068_140+5073del	ENSP00000513389.1:n.140+5068_140+5073del
ENST00000697665.1:c.93+9232_93+9237del	ENSP00000513390.1:n.93+9232_93+9237del
ENST00000697666.1:c.140+5068_140+5073del	ENSP00000513391.1:n.140+5068_140+5073del
ENST00000355622.8:c.1669_1674del MANE Select	ENSP00000363089.5:p.Met557_Thr558del
ENST00000394487.5:c.1549_1554del	ENSP00000377997.4:p.Met517_Thr518del
ENST00000472304.2:c.*1403_*1408del	ENSP00000496429.1:n.*1403_*1408del
ENST00000642985.1:c.260+5068_260+5073del	ENSP00000493686.1:n.260+5068_260+5073del
ENST00000646089.1:c.93+9232_93+9237del	ENSP00000496197.1:n.93+9232_93+9237del
ENST00000665764.1:c.93+9232_93+9237del	ENSP00000499745.1:n.93+9232_93+9237del
ENST00000355622.6:c.1669_1674del	ENSP00000363089.5:p.Met557_Thr558del
ENST00000394487.4:c.1549_1554del	ENSP00000377997.4:p.Met517_Thr518del
ENST00000472304.1:n.1586_1591del
NM_003266.3:c.1549_1554del	NP_003257.1:p.Met517_Thr518del
NM_138554.4:c.1669_1674del	NP_612564.1:p.Met557_Thr558del
NM_138557.2:c.1069_1074del	NP_612567.1:p.Met357_Thr358del
NM_138554.5:c.1669_1674del MANE Select	NP_612564.1:p.Met557_Thr558del
NM_003266.4:c.1549_1554del	NP_003257.1:p.Met517_Thr518del
NM_138557.3:c.1069_1074del	NP_612567.1:p.Met357_Thr358del