Canonical Allele Identifier: CA1875361085

Gene: TLR4

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.117718227_117718231delinsACTTT , CM000671.2:g.117718227_117718231delinsACTTT	GRCh38
NC_000009.11:g.120480505_120480509delinsACTTT , CM000671.1:g.120480505_120480509delinsACTTT	GRCh37
NC_000009.10:g.119520326_119520330delinsACTTT	NCBI36
NG_011475.1:g.19046_19050delinsACTTT
NG_011475.2:g.18825_18829delinsACTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646089.2:c.93+13662_93+13666delinsACTTT	ENSP00000496197.1:n.93+13662_93+13666delinsACTTT
ENST00000697624.1:n.200+13662_200+13666delinsACTTT
ENST00000697625.1:c.93+13662_93+13666delinsACTTT	ENSP00000513362.1:n.93+13662_93+13666delinsACTTT
ENST00000697636.1:c.93+13662_93+13666delinsACTTT	ENSP00000513366.1:n.93+13662_93+13666delinsACTTT
ENST00000697637.1:c.93+13662_93+13666delinsACTTT	ENSP00000513367.1:n.93+13662_93+13666delinsACTTT
ENST00000697664.1:c.140+9498_140+9502delinsACTTT	ENSP00000513389.1:n.140+9498_140+9502delinsACTTT
ENST00000697665.1:c.93+13662_93+13666delinsACTTT	ENSP00000513390.1:n.93+13662_93+13666delinsACTTT
ENST00000697666.1:c.140+9498_140+9502delinsACTTT	ENSP00000513391.1:n.140+9498_140+9502delinsACTTT
ENST00000355622.8:c.*3579_*3583delinsACTTT MANE Select	ENSP00000363089.5:n.*3579_*3583delinsACTTT
ENST00000642985.1:c.260+9498_260+9502delinsACTTT	ENSP00000493686.1:n.260+9498_260+9502delinsACTTT
ENST00000646089.1:c.93+13662_93+13666delinsACTTT	ENSP00000496197.1:n.93+13662_93+13666delinsACTTT
ENST00000665764.1:c.93+13662_93+13666delinsACTTT	ENSP00000499745.1:n.93+13662_93+13666delinsACTTT
NM_138554.5:c.*3579_*3583delinsACTTT MANE Select	NP_612564.1:n.*3579_*3583delinsACTTT
NM_003266.4:c.*3579_*3583delinsACTTT	NP_003257.1:n.*3579_*3583delinsACTTT
NM_138557.3:c.*3579_*3583delinsACTTT	NP_612567.1:n.*3579_*3583delinsACTTT