Canonical Allele Identifier: CA1875361183

Gene: TLR4

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.117718276_117718277delinsAG , CM000671.2:g.117718276_117718277delinsAG	GRCh38
NC_000009.11:g.120480554_120480555delinsAG , CM000671.1:g.120480554_120480555delinsAG	GRCh37
NC_000009.10:g.119520375_119520376delinsAG	NCBI36
NG_011475.1:g.19095_19096delinsAG
NG_011475.2:g.18874_18875delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646089.2:c.93+13711_93+13712delinsAG	ENSP00000496197.1:n.93+13711_93+13712delinsAG
ENST00000697624.1:n.200+13711_200+13712delinsAG
ENST00000697625.1:c.93+13711_93+13712delinsAG	ENSP00000513362.1:n.93+13711_93+13712delinsAG
ENST00000697636.1:c.93+13711_93+13712delinsAG	ENSP00000513366.1:n.93+13711_93+13712delinsAG
ENST00000697637.1:c.93+13711_93+13712delinsAG	ENSP00000513367.1:n.93+13711_93+13712delinsAG
ENST00000697664.1:c.140+9547_140+9548delinsAG	ENSP00000513389.1:n.140+9547_140+9548delinsAG
ENST00000697665.1:c.93+13711_93+13712delinsAG	ENSP00000513390.1:n.93+13711_93+13712delinsAG
ENST00000697666.1:c.140+9547_140+9548delinsAG	ENSP00000513391.1:n.140+9547_140+9548delinsAG
ENST00000355622.8:c.*3628_*3629delinsAG MANE Select	ENSP00000363089.5:n.*3628_*3629delinsAG
ENST00000642985.1:c.260+9547_260+9548delinsAG	ENSP00000493686.1:n.260+9547_260+9548delinsAG
ENST00000646089.1:c.93+13711_93+13712delinsAG	ENSP00000496197.1:n.93+13711_93+13712delinsAG
ENST00000665764.1:c.93+13711_93+13712delinsAG	ENSP00000499745.1:n.93+13711_93+13712delinsAG
NM_138554.5:c.*3628_*3629delinsAG MANE Select	NP_612564.1:n.*3628_*3629delinsAG
NM_003266.4:c.*3628_*3629delinsAG	NP_003257.1:n.*3628_*3629delinsAG
NM_138557.3:c.*3628_*3629delinsAG	NP_612567.1:n.*3628_*3629delinsAG