Canonical Allele Identifier: CA792322250

Gene: TLR3

Linked Data

• dbSNP Id: rs1402124741
• gnomAD v3: 4-186069909-C-CTGG
• gnomAD v4: 4-186069909-C-CTGG
• MyVariant Identifiers: chr4:g.186991063_186991064insTGG (hg19) ; chr4:g.186069909_186069910insTGG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186069911_186069913dup , CM000666.2:g.186069911_186069913dup	GRCh38
NC_000004.11:g.186991065_186991067dup , CM000666.1:g.186991065_186991067dup	GRCh37
NC_000004.10:g.187228059_187228061dup	NCBI36
NG_007278.1:g.5757_5759dup , LRG_117:g.5757_5759dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698351.1:c.-8+663_-8+665dup	ENSP00000513674.1:n.-8+663_-8+665dup
ENST00000698352.1:c.-8+663_-8+665dup	ENSP00000513675.1:n.-8+663_-8+665dup
ENST00000296795.8:c.-8+663_-8+665dup MANE Select	ENSP00000296795.3:n.-8+663_-8+665dup
ENST00000296795.7:c.-8+663_-8+665dup	ENSP00000296795.2:n.-8+663_-8+665dup
ENST00000513189.1:c.-8+663_-8+665dup	ENSP00000423386.1:n.-8+663_-8+665dup
NM_003265.2:c.-8+663_-8+665dup , LRG_117t1:c.-8+663_-8+665dup	NP_003256.1:n.-8+663_-8+665dup
NM_003265.3:c.-8+663_-8+665dup MANE Select	NP_003256.1:n.-8+663_-8+665dup