Canonical Allele Identifier: CA918545010

Gene: TLR4

Linked Data

• dbSNP Id: rs1588093411

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.117710442del , CM000671.2:g.117710442del	GRCh38
NC_000009.11:g.120472720del , CM000671.1:g.120472720del	GRCh37
NC_000009.10:g.119512541del	NCBI36
NG_011475.1:g.11261del
NG_011475.2:g.11040del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646089.2:c.93+5877del	ENSP00000496197.1:n.93+5877del
ENST00000697624.1:n.200+5877del
ENST00000697625.1:c.93+5877del	ENSP00000513362.1:n.93+5877del
ENST00000697636.1:c.93+5877del	ENSP00000513366.1:n.93+5877del
ENST00000697637.1:c.93+5877del	ENSP00000513367.1:n.93+5877del
ENST00000697664.1:c.140+1713del	ENSP00000513389.1:n.140+1713del
ENST00000697665.1:c.93+5877del	ENSP00000513390.1:n.93+5877del
ENST00000697666.1:c.140+1713del	ENSP00000513391.1:n.140+1713del
ENST00000355622.8:c.260+1713del MANE Select	ENSP00000363089.5:n.260+1713del
ENST00000394487.5:c.140+1713del	ENSP00000377997.4:n.140+1713del
ENST00000472304.2:c.94-1947del	ENSP00000496429.1:n.94-1947del
ENST00000642985.1:c.260+1713del	ENSP00000493686.1:n.260+1713del
ENST00000646089.1:c.93+5877del	ENSP00000496197.1:n.93+5877del
ENST00000665764.1:c.93+5877del	ENSP00000499745.1:n.93+5877del
ENST00000355622.6:c.260+1713del	ENSP00000363089.5:n.260+1713del
ENST00000394487.4:c.140+1713del	ENSP00000377997.4:n.140+1713del
ENST00000472304.1:n.178-1947del
NM_003266.3:c.140+1713del	NP_003257.1:n.140+1713del
NM_138554.4:c.260+1713del	NP_612564.1:n.260+1713del
NM_138557.2:c.-340-1947del	NP_612567.1:n.-340-1947del
NM_138554.5:c.260+1713del MANE Select	NP_612564.1:n.260+1713del
NM_003266.4:c.140+1713del	NP_003257.1:n.140+1713del
NM_138557.3:c.-340-1947del	NP_612567.1:n.-340-1947del