Canonical Allele Identifier: CA590171593

Gene: TLR4

Linked Data

• dbSNP Id: rs1392316219
• gnomAD v2: 9-120472729-C-CCTTT
• MyVariant Identifiers: chr9:g.120472730_120472731delinsCTTTTT (hg19) ; chr9:g.117710452_117710453delinsCTTTTT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.117710451_117710452insCTTT , CM000671.2:g.117710451_117710452insCTTT	GRCh38
NC_000009.11:g.120472729_120472730insCTTT , CM000671.1:g.120472729_120472730insCTTT	GRCh37
NC_000009.10:g.119512550_119512551insCTTT	NCBI36
NG_011475.1:g.11270_11271insCTTT
NG_011475.2:g.11049_11050insCTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646089.2:c.93+5886_93+5887insCTTT	ENSP00000496197.1:n.93+5886_93+5887insCTTT
ENST00000697624.1:n.200+5886_200+5887insCTTT
ENST00000697625.1:c.93+5886_93+5887insCTTT	ENSP00000513362.1:n.93+5886_93+5887insCTTT
ENST00000697636.1:c.93+5886_93+5887insCTTT	ENSP00000513366.1:n.93+5886_93+5887insCTTT
ENST00000697637.1:c.93+5886_93+5887insCTTT	ENSP00000513367.1:n.93+5886_93+5887insCTTT
ENST00000697664.1:c.140+1722_140+1723insCTTT	ENSP00000513389.1:n.140+1722_140+1723insCTTT
ENST00000697665.1:c.93+5886_93+5887insCTTT	ENSP00000513390.1:n.93+5886_93+5887insCTTT
ENST00000697666.1:c.140+1722_140+1723insCTTT	ENSP00000513391.1:n.140+1722_140+1723insCTTT
ENST00000355622.8:c.260+1722_260+1723insCTTT MANE Select	ENSP00000363089.5:n.260+1722_260+1723insCTTT
ENST00000394487.5:c.140+1722_140+1723insCTTT	ENSP00000377997.4:n.140+1722_140+1723insCTTT
ENST00000472304.2:c.94-1938_94-1937insCTTT	ENSP00000496429.1:n.94-1938_94-1937insCTTT
ENST00000642985.1:c.260+1722_260+1723insCTTT	ENSP00000493686.1:n.260+1722_260+1723insCTTT
ENST00000646089.1:c.93+5886_93+5887insCTTT	ENSP00000496197.1:n.93+5886_93+5887insCTTT
ENST00000665764.1:c.93+5886_93+5887insCTTT	ENSP00000499745.1:n.93+5886_93+5887insCTTT
ENST00000355622.6:c.260+1722_260+1723insCTTT	ENSP00000363089.5:n.260+1722_260+1723insCTTT
ENST00000394487.4:c.140+1722_140+1723insCTTT	ENSP00000377997.4:n.140+1722_140+1723insCTTT
ENST00000472304.1:n.178-1938_178-1937insCTTT
NM_003266.3:c.140+1722_140+1723insCTTT	NP_003257.1:n.140+1722_140+1723insCTTT
NM_138554.4:c.260+1722_260+1723insCTTT	NP_612564.1:n.260+1722_260+1723insCTTT
NM_138557.2:c.-340-1938_-340-1937insCTTT	NP_612567.1:n.-340-1938_-340-1937insCTTT
NM_138554.5:c.260+1722_260+1723insCTTT MANE Select	NP_612564.1:n.260+1722_260+1723insCTTT
NM_003266.4:c.140+1722_140+1723insCTTT	NP_003257.1:n.140+1722_140+1723insCTTT
NM_138557.3:c.-340-1938_-340-1937insCTTT	NP_612567.1:n.-340-1938_-340-1937insCTTT