Canonical Allele Identifier: CA108694731

Gene: TLR2

Linked Data

• dbSNP Id: rs374451575
• gnomAD v2: 4-154605469-G-A
• gnomAD v3: 4-153684317-G-A
• gnomAD v4: 4-153684317-G-A
• MyVariant Identifiers: chr4:g.154605469G>A (hg19) ; chr4:g.153684317G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.153684317G>A , CM000666.2:g.153684317G>A	GRCh38
NC_000004.11:g.154605469G>A , CM000666.1:g.154605469G>A	GRCh37
NC_000004.10:g.154824919G>A	NCBI36
NG_016229.1:g.5029G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643501.2:c.-416G>A	ENSP00000496208.2:n.-416G>A
ENST00000646219.2:c.-490G>A	ENSP00000496676.2:n.-490G>A
ENST00000646900.2:c.-191G>A	ENSP00000493968.2:n.-191G>A
ENST00000642580.1:c.-132G>A	ENSP00000495339.1:n.-132G>A
ENST00000642700.2:c.-206G>A MANE Select	ENSP00000494425.1:n.-206G>A
ENST00000643501.1:c.-416G>A	ENSP00000496208.1:n.-416G>A
ENST00000645889.1:n.28G>A
ENST00000646219.1:c.-490G>A	ENSP00000496676.1:n.-490G>A
ENST00000646900.1:c.-191G>A	ENSP00000493968.1:n.-191G>A
NM_003264.3:c.-191G>A	NP_003255.2:n.-191G>A
XM_005263194.2:c.-206G>A	XP_005263251.1:n.-206G>A
XM_005263195.2:c.-132G>A	XP_005263252.1:n.-132G>A
XM_005263196.2:c.-172G>A	XP_005263253.1:n.-172G>A
XM_005263197.2:c.-147G>A	XP_005263254.1:n.-147G>A
XM_011532215.1:c.-113G>A	XP_011530517.1:n.-113G>A
XM_011532216.1:c.-60G>A	XP_011530518.1:n.-60G>A
NM_001318787.1:c.-416G>A	NP_001305716.1:n.-416G>A
NM_001318789.1:c.-206G>A	NP_001305718.1:n.-206G>A
NM_001318790.1:c.-183G>A	NP_001305719.1:n.-183G>A
NM_001318791.1:c.-172G>A	NP_001305720.1:n.-172G>A
NM_001318793.1:c.-168G>A	NP_001305722.1:n.-168G>A
NM_001318795.1:c.-147G>A	NP_001305724.1:n.-147G>A
NM_001318796.1:c.-132G>A	NP_001305725.1:n.-132G>A
NM_003264.4:c.-191G>A	NP_003255.2:n.-191G>A
XM_011532215.2:c.-113G>A	XP_011530517.1:n.-113G>A
XM_011532216.2:c.-60G>A	XP_011530518.1:n.-60G>A
XM_017008573.1:c.-490G>A	XP_016864062.1:n.-490G>A
XM_017008574.1:c.-341G>A	XP_016864063.1:n.-341G>A
XM_017008575.1:c.-385G>A	XP_016864064.1:n.-385G>A
NM_001318787.2:c.-416G>A	NP_001305716.1:n.-416G>A
NM_001318789.2:c.-206G>A MANE Select	NP_001305718.1:n.-206G>A
NM_001318790.2:c.-183G>A	NP_001305719.1:n.-183G>A
NM_001318791.2:c.-172G>A	NP_001305720.1:n.-172G>A
NM_001318793.2:c.-168G>A	NP_001305722.1:n.-168G>A
NM_001318795.2:c.-147G>A	NP_001305724.1:n.-147G>A
NM_001318796.2:c.-132G>A	NP_001305725.1:n.-132G>A
NM_003264.5:c.-191G>A	NP_003255.2:n.-191G>A