Canonical Allele Identifier: CA590171579

Gene: TLR4

Linked Data

• dbSNP Id: rs1443756145
• gnomAD v2: 9-120472464-ATAGT-A
• MyVariant Identifiers: chr9:g.120472465_120472468del (hg19) ; chr9:g.117710187_117710190del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.117710192_117710195del , CM000671.2:g.117710192_117710195del	GRCh38
NC_000009.11:g.120472470_120472473del , CM000671.1:g.120472470_120472473del	GRCh37
NC_000009.10:g.119512291_119512294del	NCBI36
NG_011475.1:g.11011_11014del
NG_011475.2:g.10790_10793del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646089.2:c.93+5627_93+5630del	ENSP00000496197.1:n.93+5627_93+5630del
ENST00000697624.1:n.200+5627_200+5630del
ENST00000697625.1:c.93+5627_93+5630del	ENSP00000513362.1:n.93+5627_93+5630del
ENST00000697636.1:c.93+5627_93+5630del	ENSP00000513366.1:n.93+5627_93+5630del
ENST00000697637.1:c.93+5627_93+5630del	ENSP00000513367.1:n.93+5627_93+5630del
ENST00000697664.1:c.140+1463_140+1466del	ENSP00000513389.1:n.140+1463_140+1466del
ENST00000697665.1:c.93+5627_93+5630del	ENSP00000513390.1:n.93+5627_93+5630del
ENST00000697666.1:c.140+1463_140+1466del	ENSP00000513391.1:n.140+1463_140+1466del
ENST00000355622.8:c.260+1463_260+1466del MANE Select	ENSP00000363089.5:n.260+1463_260+1466del
ENST00000394487.5:c.140+1463_140+1466del	ENSP00000377997.4:n.140+1463_140+1466del
ENST00000472304.2:c.94-2197_94-2194del	ENSP00000496429.1:n.94-2197_94-2194del
ENST00000642985.1:c.260+1463_260+1466del	ENSP00000493686.1:n.260+1463_260+1466del
ENST00000646089.1:c.93+5627_93+5630del	ENSP00000496197.1:n.93+5627_93+5630del
ENST00000665764.1:c.93+5627_93+5630del	ENSP00000499745.1:n.93+5627_93+5630del
ENST00000355622.6:c.260+1463_260+1466del	ENSP00000363089.5:n.260+1463_260+1466del
ENST00000394487.4:c.140+1463_140+1466del	ENSP00000377997.4:n.140+1463_140+1466del
ENST00000472304.1:n.178-2197_178-2194del
NM_003266.3:c.140+1463_140+1466del	NP_003257.1:n.140+1463_140+1466del
NM_138554.4:c.260+1463_260+1466del	NP_612564.1:n.260+1463_260+1466del
NM_138557.2:c.-340-2197_-340-2194del	NP_612567.1:n.-340-2197_-340-2194del
NM_138554.5:c.260+1463_260+1466del MANE Select	NP_612564.1:n.260+1463_260+1466del
NM_003266.4:c.140+1463_140+1466del	NP_003257.1:n.140+1463_140+1466del
NM_138557.3:c.-340-2197_-340-2194del	NP_612567.1:n.-340-2197_-340-2194del