Canonical Allele Identifier: CA112098133
Gene: TLR3 HGNC NCBI
MyVariant.info:
Revel Score:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186083063C>A , CM000666.2:g.186083063C>A GRCh38
NC_000004.11:g.187004217C>A , CM000666.1:g.187004217C>A GRCh37
NC_000004.10:g.187241211C>A NCBI36
NG_007278.1:g.18909C>A , LRG_117:g.18909C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000508051.2:c.546C>A ENSP00000513677.1:p.Phe182Leu
ENST00000698351.1:c.864+513C>A ENSP00000513674.1:n.864+513C>A
ENST00000698352.1:c.*929C>A ENSP00000513675.1:n.*929C>A
ENST00000698353.1:n.1252C>A
ENST00000698354.1:c.546C>A ENSP00000513676.1:p.Phe182Leu
ENST00000296795.8:c.1377C>A MANE Select ENSP00000296795.3:p.Phe459Leu
ENST00000296795.7:c.1377C>A ENSP00000296795.2:p.Phe459Leu
ENST00000504367.1:c.546C>A ENSP00000423684.1:p.Phe182Leu
ENST00000512264.1:n.1453C>A
NM_003265.2:c.1377C>A , LRG_117t1:c.1377C>A NP_003256.1:p.Phe459Leu
NM_003265.3:c.1377C>A MANE Select NP_003256.1:p.Phe459Leu