Canonical Allele Identifier: CA1875363082

Gene: TLR4

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.117721660_117721661delinsCT , CM000671.2:g.117721660_117721661delinsCT	GRCh38
NC_000009.11:g.120483938_120483939delinsCT , CM000671.1:g.120483938_120483939delinsCT	GRCh37
NC_000009.10:g.119523759_119523760delinsCT	NCBI36
NG_011475.2:g.22258_22259delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646089.2:c.93+17095_93+17096delinsCT	ENSP00000496197.1:n.93+17095_93+17096delinsCT
ENST00000697624.1:n.200+17095_200+17096delinsCT
ENST00000697625.1:c.93+17095_93+17096delinsCT	ENSP00000513362.1:n.93+17095_93+17096delinsCT
ENST00000697636.1:c.93+17095_93+17096delinsCT	ENSP00000513366.1:n.93+17095_93+17096delinsCT
ENST00000697637.1:c.93+17095_93+17096delinsCT	ENSP00000513367.1:n.93+17095_93+17096delinsCT
ENST00000697664.1:c.140+12931_140+12932delinsCT	ENSP00000513389.1:n.140+12931_140+12932delinsCT
ENST00000697665.1:c.93+17095_93+17096delinsCT	ENSP00000513390.1:n.93+17095_93+17096delinsCT
ENST00000697666.1:c.140+12931_140+12932delinsCT	ENSP00000513391.1:n.140+12931_140+12932delinsCT
ENST00000355622.8:c.*7012_*7013delinsCT MANE Select	ENSP00000363089.5:n.*7012_*7013delinsCT
ENST00000642985.1:c.260+12931_260+12932delinsCT	ENSP00000493686.1:n.260+12931_260+12932delinsCT
ENST00000646089.1:c.93+17095_93+17096delinsCT	ENSP00000496197.1:n.93+17095_93+17096delinsCT
ENST00000665764.1:c.93+17095_93+17096delinsCT	ENSP00000499745.1:n.93+17095_93+17096delinsCT
NM_138554.5:c.*7012_*7013delinsCT MANE Select	NP_612564.1:n.*7012_*7013delinsCT
NM_003266.4:c.*7012_*7013delinsCT	NP_003257.1:n.*7012_*7013delinsCT
NM_138557.3:c.*7012_*7013delinsCT	NP_612567.1:n.*7012_*7013delinsCT