Canonical Allele Identifier: CA792307250
Gene: TLR3 HGNC NCBI

Linked Data

dbSNP Id: rs1435892786
gnomAD v3: 4-186086062-C-CT
gnomAD v4: 4-186086062-C-CT
MyVariant Identifiers: chr4:g.187007216_187007217insT (hg19) chr4:g.186086062_186086063insT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186086062_186086063insT , CM000666.2:g.186086062_186086063insT GRCh38
NC_000004.11:g.187007216_187007217insT , CM000666.1:g.187007216_187007217insT GRCh37
NC_000004.10:g.187244210_187244211insT NCBI36
NG_007278.1:g.21908_21909insT , LRG_117:g.21908_21909insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000698352.1:c.*3456_*3457insT ENSP00000513675.1:n.*3456_*3457insT
ENST00000698353.1:n.3779_3780insT
ENST00000698354.1:c.*1189_*1190insT ENSP00000513676.1:n.*1189_*1190insT
ENST00000296795.8:c.*1189_*1190insT MANE Select ENSP00000296795.3:n.*1189_*1190insT
ENST00000296795.7:c.*1189_*1190insT ENSP00000296795.2:n.*1189_*1190insT
NM_003265.3:c.*1189_*1190insT MANE Select NP_003256.1:n.*1189_*1190insT
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