Canonical Allele Identifier: CA590171909

Gene: TLR4

Linked Data

• dbSNP Id: rs1210481231
• gnomAD v2: 9-120480892-CTG-C
• gnomAD v3: 9-117718614-CTG-C
• gnomAD v4: 9-117718614-CTG-C
• MyVariant Identifiers: chr9:g.120480893_120480894del (hg19) ; chr9:g.117718615_117718616del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.117718619_117718620del , CM000671.2:g.117718619_117718620del	GRCh38
NC_000009.11:g.120480897_120480898del , CM000671.1:g.120480897_120480898del	GRCh37
NC_000009.10:g.119520718_119520719del	NCBI36
NG_011475.1:g.19438_19439del
NG_011475.2:g.19217_19218del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646089.2:c.93+14054_93+14055del	ENSP00000496197.1:n.93+14054_93+14055del
ENST00000697624.1:n.200+14054_200+14055del
ENST00000697625.1:c.93+14054_93+14055del	ENSP00000513362.1:n.93+14054_93+14055del
ENST00000697636.1:c.93+14054_93+14055del	ENSP00000513366.1:n.93+14054_93+14055del
ENST00000697637.1:c.93+14054_93+14055del	ENSP00000513367.1:n.93+14054_93+14055del
ENST00000697664.1:c.140+9890_140+9891del	ENSP00000513389.1:n.140+9890_140+9891del
ENST00000697665.1:c.93+14054_93+14055del	ENSP00000513390.1:n.93+14054_93+14055del
ENST00000697666.1:c.140+9890_140+9891del	ENSP00000513391.1:n.140+9890_140+9891del
ENST00000355622.8:c.*3971_*3972del MANE Select	ENSP00000363089.5:n.*3971_*3972del
ENST00000642985.1:c.260+9890_260+9891del	ENSP00000493686.1:n.260+9890_260+9891del
ENST00000646089.1:c.93+14054_93+14055del	ENSP00000496197.1:n.93+14054_93+14055del
ENST00000665764.1:c.93+14054_93+14055del	ENSP00000499745.1:n.93+14054_93+14055del
NM_138554.5:c.*3971_*3972del MANE Select	NP_612564.1:n.*3971_*3972del
NM_003266.4:c.*3971_*3972del	NP_003257.1:n.*3971_*3972del
NM_138557.3:c.*3971_*3972del	NP_612567.1:n.*3971_*3972del