Canonical Allele Identifier: CA2707184510

Gene: TLR2

Linked Data

• dbSNP Id: rs111200466

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.153684316_153684338dup , CM000666.2:g.153684316_153684338dup	GRCh38
NC_000004.11:g.154605468_154605490dup , CM000666.1:g.154605468_154605490dup	GRCh37
NC_000004.10:g.154824918_154824940dup	NCBI36
NG_016229.1:g.5028_5050dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000643501.2:c.-417_-395dup	ENSP00000496208.2:n.-417_-395dup
ENST00000646219.2:c.-491_-469dup	ENSP00000496676.2:n.-491_-469dup
ENST00000646900.2:c.-192_-170dup	ENSP00000493968.2:n.-192_-170dup
ENST00000642580.1:c.-133_-111dup	ENSP00000495339.1:n.-133_-111dup
ENST00000642700.2:c.-207_-185dup MANE Select	ENSP00000494425.1:n.-207_-185dup
ENST00000643501.1:c.-417_-395dup	ENSP00000496208.1:n.-417_-395dup
ENST00000645889.1:n.27_49dup
ENST00000646219.1:c.-491_-469dup	ENSP00000496676.1:n.-491_-469dup
ENST00000646900.1:c.-192_-170dup	ENSP00000493968.1:n.-192_-170dup
NM_003264.3:c.-192_-170dup	NP_003255.2:n.-192_-170dup
XM_005263194.2:c.-207_-185dup	XP_005263251.1:n.-207_-185dup
XM_005263195.2:c.-133_-111dup	XP_005263252.1:n.-133_-111dup
XM_005263196.2:c.-173_-151dup	XP_005263253.1:n.-173_-151dup
XM_005263197.2:c.-148_-126dup	XP_005263254.1:n.-148_-126dup
XM_011532215.1:c.-114_-92dup	XP_011530517.1:n.-114_-92dup
XM_011532216.1:c.-61_-39dup	XP_011530518.1:n.-61_-39dup
NM_001318787.1:c.-417_-395dup	NP_001305716.1:n.-417_-395dup
NM_001318789.1:c.-207_-185dup	NP_001305718.1:n.-207_-185dup
NM_001318790.1:c.-184_-163+1dup
NM_001318791.1:c.-173_-151dup	NP_001305720.1:n.-173_-151dup
NM_001318793.1:c.-169_-148+1dup
NM_001318795.1:c.-148_-126dup	NP_001305724.1:n.-148_-126dup
NM_001318796.1:c.-133_-111dup	NP_001305725.1:n.-133_-111dup
NM_003264.4:c.-192_-170dup	NP_003255.2:n.-192_-170dup
XM_011532215.2:c.-114_-92dup	XP_011530517.1:n.-114_-92dup
XM_011532216.2:c.-61_-39dup	XP_011530518.1:n.-61_-39dup
XM_017008573.1:c.-491_-469dup	XP_016864062.1:n.-491_-469dup
XM_017008574.1:c.-342_-320dup	XP_016864063.1:n.-342_-320dup
XM_017008575.1:c.-386_-364dup	XP_016864064.1:n.-386_-364dup
NM_001318787.2:c.-417_-395dup	NP_001305716.1:n.-417_-395dup
NM_001318789.2:c.-207_-185dup MANE Select	NP_001305718.1:n.-207_-185dup
NM_001318790.2:c.-184_-163+1dup
NM_001318791.2:c.-173_-151dup	NP_001305720.1:n.-173_-151dup
NM_001318793.2:c.-169_-148+1dup
NM_001318795.2:c.-148_-126dup	NP_001305724.1:n.-148_-126dup
NM_001318796.2:c.-133_-111dup	NP_001305725.1:n.-133_-111dup
NM_003264.5:c.-192_-170dup	NP_003255.2:n.-192_-170dup