Canonical Allele Identifier: CA792306872
Gene: TLR3 HGNC NCBI

Linked Data

dbSNP Id: rs1260875908
gnomAD v3: 4-186085402-A-AT
gnomAD v4: 4-186085402-A-AT
MyVariant Identifiers: chr4:g.187006556_187006557insT (hg19) chr4:g.186085402_186085403insT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186085408dup , CM000666.2:g.186085408dup GRCh38
NC_000004.11:g.187006562dup , CM000666.1:g.187006562dup GRCh37
NC_000004.10:g.187243556dup NCBI36
NG_007278.1:g.21254dup , LRG_117:g.21254dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000698352.1:c.*2802dup ENSP00000513675.1:n.*2802dup
ENST00000698353.1:n.3125dup
ENST00000698354.1:c.*535dup ENSP00000513676.1:n.*535dup
ENST00000296795.8:c.*535dup MANE Select ENSP00000296795.3:n.*535dup
ENST00000296795.7:c.*535dup ENSP00000296795.2:n.*535dup
NM_003265.3:c.*535dup MANE Select NP_003256.1:n.*535dup
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