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.
mRNA and Protein(s)
-
NM_001279.4 → NP_001270.1 lipid transferase CIDEA isoform 1
See identical proteins and their annotated locations for NP_001270.1
Status: REVIEWED
- Description
- Transcript Variant: This variant (1) encodes the shorter isoform (1).
- Source sequence(s)
-
BC031896, BQ718688, R73455
- Consensus CDS
-
CCDS11856.1
- UniProtKB/Swiss-Prot
- B0YIY7, O60543, Q6UPR7
- Related
- ENSP00000320209.8, ENST00000320477.10
- Conserved Domains (1) summary
-
- cd06539
Location:33 → 110
- CIDE_N_A; CIDE_N domain of CIDE-A proteins. The CIDE_N (cell death-inducing DFF45-like effector, N-terminal) domain is found at the N-terminus of the CIDE (cell death-inducing DFF45-like effector) proteins. These proteins are associated with the chromatin ...
-
NM_001318383.2 → NP_001305312.1 lipid transferase CIDEA isoform 2
Status: REVIEWED
- Description
- Transcript Variant: This variant (2) differs in the 5' UTR and uses an alternate start codon, compared to variant 1. The encoded isoform (2) has a longer and distinct N-terminus than isoform 1.
- Source sequence(s)
-
AK122762, AP005264, BC031896
- UniProtKB/TrEMBL
-
Q8N5P9
- Conserved Domains (1) summary
-
- cd06539
Location:67 → 144
- CIDE_N_A; CIDE_N domain of CIDE-A proteins. The CIDE_N (cell death-inducing DFF45-like effector, N-terminal) domain is found at the N-terminus of the CIDE (cell death-inducing DFF45-like effector) proteins. These proteins are associated with the chromatin ...
RNA
-
NR_134607.2 RNA Sequence
Status: REVIEWED
- Description
- Transcript Variant: This variant (3) uses an alternate splice site and contains an alternate internal exon, compared to variant 1. This variant is represented as non-coding because the use of the 5'-most supported translational start codon renders the transcript a candidate for nonsense-mediated mRNA decay (NMD).
- Source sequence(s)
-
AK122762, AP005264, BC031896, BQ718688
- Related
-
ENST00000522713.5
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_000018.10 Reference GRCh38.p14 Primary Assembly
- Range
-
12254361..12277595
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)
Alternate T2T-CHM13v2.0
Genomic
-
NC_060942.1 Alternate T2T-CHM13v2.0
- Range
-
12417352..12440590
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)