Canonical Allele Identifier: CA1519841718
Gene: TLR3 HGNC NCBI

Linked Data

dbSNP Id: rs2099301141

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186069887del , CM000666.2:g.186069887del GRCh38
NC_000004.11:g.186991041del , CM000666.1:g.186991041del GRCh37
NC_000004.10:g.187228035del NCBI36
NG_007278.1:g.5733del , LRG_117:g.5733del

Transcript Alleles

HGVS Amino-acid change
ENST00000698351.1:c.-8+639del ENSP00000513674.1:n.-8+639del
ENST00000698352.1:c.-8+639del ENSP00000513675.1:n.-8+639del
ENST00000296795.8:c.-8+639del MANE Select ENSP00000296795.3:n.-8+639del
ENST00000296795.7:c.-8+639del ENSP00000296795.2:n.-8+639del
ENST00000513189.1:c.-8+639del ENSP00000423386.1:n.-8+639del
NM_003265.2:c.-8+639del , LRG_117t1:c.-8+639del NP_003256.1:n.-8+639del
NM_003265.3:c.-8+639del MANE Select NP_003256.1:n.-8+639del