NEW
Try the new Transcript table
These reference sequences exist independently of genome builds. Explain
These reference sequences are curated independently of the genome
annotation cycle, so their versions may not match the RefSeq versions in the current
genome build. Identify version mismatches by comparing the version of the RefSeq in
this section to the one reported in Genomic regions,
transcripts, and products above.
Genomic
-
NG_011523.1 RefSeqGene
- Range
-
5007..16847
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)
mRNA and Protein(s)
-
NM_001039661.2 → NP_001034750.1 toll/interleukin-1 receptor domain-containing adapter protein isoform a
See identical proteins and their annotated locations for NP_001034750.1
Status: REVIEWED
- Description
- Transcript Variant: This variant (3) represents the longer transcript but encodes the shorter isoform (a). Variants 3 and 5 both encode the same isoform (a).
- Source sequence(s)
-
AK124298, AP001318, BC032474
- Consensus CDS
-
CCDS8472.1
- UniProtKB/Swiss-Prot
- B3KW65, P58753, Q56UH9, Q56UI0, Q8N5E5
- Related
- ENSP00000376447.2, ENST00000392680.6
- Conserved Domains (1) summary
-
- pfam13676
Location:88 → 208
- TIR_2; TIR domain
-
NM_001318776.2 → NP_001305705.1 toll/interleukin-1 receptor domain-containing adapter protein isoform b
Status: REVIEWED
- Description
- Transcript Variant: This variant (4) differs in the 5' UTR compared to variant 2. Variants 2 and 4 both encode the same isoform (b).
- Source sequence(s)
-
AF378129, AK124298, AK313147
- Consensus CDS
-
CCDS41731.1
- UniProtKB/Swiss-Prot
-
P58753
- Related
- ENSP00000515019.1, ENST00000700491.1
- Conserved Domains (1) summary
-
- pfam13676
Location:88 → 208
- TIR_2; TIR domain
-
NM_001318777.2 → NP_001305706.1 toll/interleukin-1 receptor domain-containing adapter protein isoform a
Status: REVIEWED
- Description
- Transcript Variant: This variant (5) differs in the 5' UTR compared to variant 3. Variants 3 and 5 both encode the same isoform (a).
- Source sequence(s)
-
AK124298, AP001318, AY576785
- Consensus CDS
-
CCDS8472.1
- UniProtKB/Swiss-Prot
- B3KW65, P58753, Q56UH9, Q56UI0, Q8N5E5
- Related
- ENSP00000376446.1, ENST00000392679.6
- Conserved Domains (1) summary
-
- pfam13676
Location:88 → 208
- TIR_2; TIR domain
-
NM_148910.3 → NP_683708.1 toll/interleukin-1 receptor domain-containing adapter protein isoform b
See identical proteins and their annotated locations for NP_683708.1
Status: REVIEWED
- Description
- Transcript Variant: This variant (2) has an additional segment within the 5' UTR and differs in the 3' coding region and 3' UTR, compared to variant 3. This results in a longer isoform (b) with a distinct C-terminus, compared to isoform a. Variants 2 and 4 both encode the same isoform (b).
- Source sequence(s)
-
AF378129, AK124298
- Consensus CDS
-
CCDS41731.1
- UniProtKB/Swiss-Prot
-
P58753
- Related
- ENSP00000376445.3, ENST00000392678.7
- Conserved Domains (1) summary
-
- pfam13676
Location:88 → 208
- TIR_2; TIR domain
The following sections contain reference sequences that belong to a
specific genome build. Explain
This section includes genomic Reference
Sequences (RefSeqs) from all assemblies on which this gene is annotated, such as
RefSeqs for chromosomes and scaffolds (contigs) from both reference and alternate
assemblies. Model RNAs and proteins are also reported here.
Reference GRCh38.p14 Primary Assembly
Genomic
-
NC_000011.10 Reference GRCh38.p14 Primary Assembly
- Range
-
126283093..126294933
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)
Alternate T2T-CHM13v2.0
Genomic
-
NC_060935.1 Alternate T2T-CHM13v2.0
- Range
-
126314493..126326362
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)
The following Reference Sequences have been suppressed. Explain
These RefSeqs were suppressed for the
cited reason(s). Suppressed RefSeqs do not appear in BLAST databases, related
sequence links, or BLAST links (BLink), but may still be retrieved by clicking on
their accession.version below.
-
NM_052887.2: Suppressed sequence
- Description
- NM_052887.2: This RefSeq was permanently suppressed because it is a nonsense-mediated mRNA decay (NMD) candidate.