Canonical Allele Identifier: CA1875361091

Gene: TLR4

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.117718228_117718229delinsCT , CM000671.2:g.117718228_117718229delinsCT	GRCh38
NC_000009.11:g.120480506_120480507delinsCT , CM000671.1:g.120480506_120480507delinsCT	GRCh37
NC_000009.10:g.119520327_119520328delinsCT	NCBI36
NG_011475.1:g.19047_19048delinsCT
NG_011475.2:g.18826_18827delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646089.2:c.93+13663_93+13664delinsCT	ENSP00000496197.1:n.93+13663_93+13664delinsCT
ENST00000697624.1:n.200+13663_200+13664delinsCT
ENST00000697625.1:c.93+13663_93+13664delinsCT	ENSP00000513362.1:n.93+13663_93+13664delinsCT
ENST00000697636.1:c.93+13663_93+13664delinsCT	ENSP00000513366.1:n.93+13663_93+13664delinsCT
ENST00000697637.1:c.93+13663_93+13664delinsCT	ENSP00000513367.1:n.93+13663_93+13664delinsCT
ENST00000697664.1:c.140+9499_140+9500delinsCT	ENSP00000513389.1:n.140+9499_140+9500delinsCT
ENST00000697665.1:c.93+13663_93+13664delinsCT	ENSP00000513390.1:n.93+13663_93+13664delinsCT
ENST00000697666.1:c.140+9499_140+9500delinsCT	ENSP00000513391.1:n.140+9499_140+9500delinsCT
ENST00000355622.8:c.*3580_*3581delinsCT MANE Select	ENSP00000363089.5:n.*3580_*3581delinsCT
ENST00000642985.1:c.260+9499_260+9500delinsCT	ENSP00000493686.1:n.260+9499_260+9500delinsCT
ENST00000646089.1:c.93+13663_93+13664delinsCT	ENSP00000496197.1:n.93+13663_93+13664delinsCT
ENST00000665764.1:c.93+13663_93+13664delinsCT	ENSP00000499745.1:n.93+13663_93+13664delinsCT
NM_138554.5:c.*3580_*3581delinsCT MANE Select	NP_612564.1:n.*3580_*3581delinsCT
NM_003266.4:c.*3580_*3581delinsCT	NP_003257.1:n.*3580_*3581delinsCT
NM_138557.3:c.*3580_*3581delinsCT	NP_612567.1:n.*3580_*3581delinsCT