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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_021398.1 RefSeqGene
- Range
-
5032..11561
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)
mRNA and Protein(s)
-
NM_001178054.2 → NP_001171525.1 tachykinin-3 isoform 2 precursor
See identical proteins and their annotated locations for NP_001171525.1
Status: REVIEWED
- Description
- Transcript Variant: This variant (2) lacks an in-frame exon in the coding region, compared to variant 1. The encoded isoform (2) is shorter and lacks the entire Neurokinin-B peptide compared to isoform 1. The encoded isoform (2) and may undergo proteolytic processing similar to isoform 1.
- Source sequence(s)
-
AF537121, BE500999, BP212420
- Consensus CDS
-
CCDS53803.1
- Related
- ENSP00000408208.1, ENST00000441881.5
- Conserved Domains (1) summary
-
- pfam03823
Location:1 → 53
- Neurokinin_B; Neurokinin B
-
NM_013251.4 → NP_037383.1 tachykinin-3 isoform 1 preproprotein
See identical proteins and their annotated locations for NP_037383.1
Status: REVIEWED
- Description
- Transcript Variant: This variant (1) encodes the longer isoform (1).
- Source sequence(s)
-
BC032145
- Consensus CDS
-
CCDS8928.1
- UniProtKB/Swiss-Prot
- Q6IAG2, Q71BC6, Q71BC9, Q9UHF0
- Related
- ENSP00000404056.2, ENST00000458521.7
- Conserved Domains (1) summary
-
- pfam03823
Location:1 → 54
- Neurokinin_B; Neurokinin B
RNA
-
NR_033654.2 RNA Sequence
Status: REVIEWED
- Description
- Transcript Variant: This variant (3) has an additional internal exon, compared to variant 1. This variant is represented as non-coding because the use of the 5'-most supported translational start codon, as used in variant 1, renders the transcript a candidate for nonsense-mediated mRNA decay (NMD).
- Source sequence(s)
-
AY358679
- Related
-
ENST00000357616.7
-
NR_135164.2 RNA Sequence
Status: REVIEWED
- Description
- Transcript Variant: This variant (4) contains two alternate internal exons resulting in a longer transcript compared to variant 1. This variant is represented as non-coding because the use of the 5'-most supported translational start codon, as used in variant 1, renders the transcript a candidate for nonsense-mediated mRNA decay (NMD).
- Source sequence(s)
-
AF537114, BE500999, BP212420
- Related
-
ENST00000438756.5
-
NR_135165.2 RNA Sequence
Status: REVIEWED
- Description
- Transcript Variant: This variant (5) contains an alternate internal exon resulting in a longer transcript compared to variant 1. This variant is represented as non-coding because the use of the 5'-most supported translational start codon, as used in variant 1, renders the transcript a candidate for nonsense-mediated mRNA decay (NMD).
- Source sequence(s)
-
AF537117, BE500999, BP212420
-
NR_135166.2 RNA Sequence
Status: REVIEWED
- Description
- Transcript Variant: This variant (6) lacks an alternate exon and contains an alternate exon resulting in a longer transcript compared to variant 1. This variant is represented as non-coding because the use of the 5'-most supported translational start codon, as used in variant 1, renders the transcript a candidate for nonsense-mediated mRNA decay (NMD).
- Source sequence(s)
-
AF537120, BE500999, BP212420
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_000012.12 Reference GRCh38.p14 Primary Assembly
- Range
-
57010000..57016529 complement
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)
Alternate T2T-CHM13v2.0
Genomic
-
NC_060936.1 Alternate T2T-CHM13v2.0
- Range
-
56977869..56984399 complement
- 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_001006667.1: Suppressed sequence
- Description
- NM_001006667.1: This RefSeq was permanently suppressed because it is a nonsense-mediated mRNA decay (NMD) candidate.