Canonical Allele Identifier: CA1069671924

Gene: TLR2

Linked Data

• gnomAD v3: 4-153687204-AGTGC-A
• gnomAD v4: 4-153687204-AGTGC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.153687205_153687208del , CM000666.2:g.153687205_153687208del	GRCh38
NC_000004.11:g.154608357_154608360del , CM000666.1:g.154608357_154608360del	GRCh37
NC_000004.10:g.154827807_154827810del	NCBI36
NG_016229.1:g.7917_7920del

Transcript Alleles

HGVS	Amino-acid change
ENST00000643501.2:c.-372-712_-372-709del	ENSP00000496208.2:n.-372-712_-372-709del
ENST00000646219.2:c.-446-697_-446-694del	ENSP00000496676.2:n.-446-697_-446-694del
ENST00000646900.2:c.-147-712_-147-709del	ENSP00000493968.2:n.-147-712_-147-709del
ENST00000642580.1:c.-88-712_-88-709del	ENSP00000495339.1:n.-88-712_-88-709del
ENST00000642700.2:c.-162-697_-162-694del MANE Select	ENSP00000494425.1:n.-162-697_-162-694del
ENST00000643501.1:c.-372-712_-372-709del	ENSP00000496208.1:n.-372-712_-372-709del
ENST00000645889.1:n.72-697_72-694del
ENST00000646219.1:c.-446-697_-446-694del	ENSP00000496676.1:n.-446-697_-446-694del
ENST00000646900.1:c.-147-712_-147-709del	ENSP00000493968.1:n.-147-712_-147-709del
NM_003264.3:c.-147-712_-147-709del	NP_003255.2:n.-147-712_-147-709del
XM_005263194.2:c.-162-697_-162-694del	XP_005263251.1:n.-162-697_-162-694del
XM_005263195.2:c.-88-712_-88-709del	XP_005263252.1:n.-88-712_-88-709del
XM_005263196.2:c.-128-731_-128-728del	XP_005263253.1:n.-128-731_-128-728del
XM_005263197.2:c.-103-697_-103-694del	XP_005263254.1:n.-103-697_-103-694del
XM_011532215.1:c.-69-731_-69-728del	XP_011530517.1:n.-69-731_-69-728del
XM_011532216.1:c.-17+2845_-17+2848del	XP_011530518.1:n.-17+2845_-17+2848del
NM_001318787.1:c.-372-712_-372-709del	NP_001305716.1:n.-372-712_-372-709del
NM_001318789.1:c.-162-697_-162-694del	NP_001305718.1:n.-162-697_-162-694del
NM_001318790.1:c.-162-697_-162-694del	NP_001305719.1:n.-162-697_-162-694del
NM_001318791.1:c.-128-731_-128-728del	NP_001305720.1:n.-128-731_-128-728del
NM_001318793.1:c.-147-712_-147-709del	NP_001305722.1:n.-147-712_-147-709del
NM_001318795.1:c.-103-697_-103-694del	NP_001305724.1:n.-103-697_-103-694del
NM_001318796.1:c.-88-712_-88-709del	NP_001305725.1:n.-88-712_-88-709del
NM_003264.4:c.-147-712_-147-709del	NP_003255.2:n.-147-712_-147-709del
XM_011532215.2:c.-69-731_-69-728del	XP_011530517.1:n.-69-731_-69-728del
XM_011532216.2:c.-17+2845_-17+2848del	XP_011530518.1:n.-17+2845_-17+2848del
XM_017008573.1:c.-446-697_-446-694del	XP_016864062.1:n.-446-697_-446-694del
XM_017008574.1:c.-297-697_-297-694del	XP_016864063.1:n.-297-697_-297-694del
XM_017008575.1:c.-341-712_-341-709del	XP_016864064.1:n.-341-712_-341-709del
NM_001318787.2:c.-372-712_-372-709del	NP_001305716.1:n.-372-712_-372-709del
NM_001318789.2:c.-162-697_-162-694del MANE Select	NP_001305718.1:n.-162-697_-162-694del
NM_001318790.2:c.-162-697_-162-694del	NP_001305719.1:n.-162-697_-162-694del
NM_001318791.2:c.-128-731_-128-728del	NP_001305720.1:n.-128-731_-128-728del
NM_001318793.2:c.-147-712_-147-709del	NP_001305722.1:n.-147-712_-147-709del
NM_001318795.2:c.-103-697_-103-694del	NP_001305724.1:n.-103-697_-103-694del
NM_001318796.2:c.-88-712_-88-709del	NP_001305725.1:n.-88-712_-88-709del
NM_003264.5:c.-147-712_-147-709del	NP_003255.2:n.-147-712_-147-709del