Canonical Allele Identifier: CA590171902

Gene: TLR4

Linked Data

• gnomAD v2: 9-120480740-TAATC-T
• gnomAD v3: 9-117718462-TAATC-T
• gnomAD v4: 9-117718462-TAATC-T
• MyVariant Identifiers: chr9:g.120480741_120480744del (hg19) ; chr9:g.117718463_117718466del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.117718466_117718469del , CM000671.2:g.117718466_117718469del	GRCh38
NC_000009.11:g.120480744_120480747del , CM000671.1:g.120480744_120480747del	GRCh37
NC_000009.10:g.119520565_119520568del	NCBI36
NG_011475.1:g.19285_19288del
NG_011475.2:g.19064_19067del

Transcript Alleles

HGVS	Amino-acid change
ENST00000646089.2:c.93+13901_93+13904del	ENSP00000496197.1:n.93+13901_93+13904del
ENST00000697624.1:n.200+13901_200+13904del
ENST00000697625.1:c.93+13901_93+13904del	ENSP00000513362.1:n.93+13901_93+13904del
ENST00000697636.1:c.93+13901_93+13904del	ENSP00000513366.1:n.93+13901_93+13904del
ENST00000697637.1:c.93+13901_93+13904del	ENSP00000513367.1:n.93+13901_93+13904del
ENST00000697664.1:c.140+9737_140+9740del	ENSP00000513389.1:n.140+9737_140+9740del
ENST00000697665.1:c.93+13901_93+13904del	ENSP00000513390.1:n.93+13901_93+13904del
ENST00000697666.1:c.140+9737_140+9740del	ENSP00000513391.1:n.140+9737_140+9740del
ENST00000355622.8:c.*3818_*3821del MANE Select	ENSP00000363089.5:n.*3818_*3821del
ENST00000642985.1:c.260+9737_260+9740del	ENSP00000493686.1:n.260+9737_260+9740del
ENST00000646089.1:c.93+13901_93+13904del	ENSP00000496197.1:n.93+13901_93+13904del
ENST00000665764.1:c.93+13901_93+13904del	ENSP00000499745.1:n.93+13901_93+13904del
NM_138554.5:c.*3818_*3821del MANE Select	NP_612564.1:n.*3818_*3821del
NM_003266.4:c.*3818_*3821del	NP_003257.1:n.*3818_*3821del
NM_138557.3:c.*3818_*3821del	NP_612567.1:n.*3818_*3821del