Canonical Allele Identifier: CA2505172937

Gene: TLR4

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.117718463_117718464insTAA , CM000671.2:g.117718463_117718464insTAA	GRCh38
NC_000009.11:g.120480741_120480742insTAA , CM000671.1:g.120480741_120480742insTAA	GRCh37
NC_000009.10:g.119520562_119520563insTAA	NCBI36
NG_011475.1:g.19282_19283insTAA
NG_011475.2:g.19061_19062insTAA

Transcript Alleles

HGVS	Amino-acid change
ENST00000646089.2:c.93+13898_93+13899insTAA	ENSP00000496197.1:n.93+13898_93+13899insT...
ENST00000697624.1:n.200+13898_200+13899insTAA
ENST00000697625.1:c.93+13898_93+13899insTAA	ENSP00000513362.1:n.93+13898_93+13899insT...
ENST00000697636.1:c.93+13898_93+13899insTAA	ENSP00000513366.1:n.93+13898_93+13899insT...
ENST00000697637.1:c.93+13898_93+13899insTAA	ENSP00000513367.1:n.93+13898_93+13899insT...
ENST00000697664.1:c.140+9734_140+9735insTAA	ENSP00000513389.1:n.140+9734_140+9735insT...
ENST00000697665.1:c.93+13898_93+13899insTAA	ENSP00000513390.1:n.93+13898_93+13899insT...
ENST00000697666.1:c.140+9734_140+9735insTAA	ENSP00000513391.1:n.140+9734_140+9735insT...
ENST00000355622.8:c.*3815_*3816insTAA MANE Select	ENSP00000363089.5:n.*3815_*3816insTAA
ENST00000642985.1:c.260+9734_260+9735insTAA	ENSP00000493686.1:n.260+9734_260+9735insT...
ENST00000646089.1:c.93+13898_93+13899insTAA	ENSP00000496197.1:n.93+13898_93+13899insT...
ENST00000665764.1:c.93+13898_93+13899insTAA	ENSP00000499745.1:n.93+13898_93+13899insT...
NM_138554.5:c.*3815_*3816insTAA MANE Select	NP_612564.1:n.*3815_*3816insTAA
NM_003266.4:c.*3815_*3816insTAA	NP_003257.1:n.*3815_*3816insTAA
NM_138557.3:c.*3815_*3816insTAA	NP_612567.1:n.*3815_*3816insTAA