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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.
mRNA and Protein(s)
-
NM_001039670.3 → NP_001034759.1 non-homologous end joining factor IFFO1 isoform 4
See identical proteins and their annotated locations for NP_001034759.1
Status: REVIEWED
- Description
- Transcript Variant: This variant (4) uses an alternate in-frame splice site in the central coding region, compared to variant 2, resulting in an isoform (4) that is 1 aa longer than isoform 2.
- Source sequence(s)
-
AC006064, AI969315, BC002857, BC063004, BC110387
- Consensus CDS
-
CCDS41741.1
- UniProtKB/Swiss-Prot
-
Q0D2I5
- UniProtKB/TrEMBL
-
Q6P593
- Related
- ENSP00000349364.4, ENST00000356896.8
- Conserved Domains (1) summary
-
- pfam00038
Location:230 → 522
- Filament; Intermediate filament protein
-
NM_001193457.2 → NP_001180386.1 non-homologous end joining factor IFFO1 isoform 5
See identical proteins and their annotated locations for NP_001180386.1
Status: REVIEWED
- Description
- Transcript Variant: This variant (5) uses two alternate in-frame splice sites in the central coding region, compared to variant 2, resulting in an isoform (5) that is longer than isoform 2.
- Source sequence(s)
-
AI423929, AK298905, AL080214, BC063004, DA744744, DA969856
- Consensus CDS
-
CCDS73425.1
- UniProtKB/TrEMBL
-
A0A087WZ16
- Related
- ENSP00000482285.1, ENST00000619571.5
- Conserved Domains (1) summary
-
- pfam00038
Location:230 → 530
- Filament; Intermediate filament protein
-
NM_001330324.2 → NP_001317253.1 non-homologous end joining factor IFFO1 isoform 7
Status: REVIEWED
- Description
- Transcript Variant: This variant (8) lacks an alternate in-frame exon in the central coding region, compared to variant 2, resulting in an isoform (7) that is 3 aa shorter than isoform 2.
- Source sequence(s)
-
AA251428, AC006064, AF124432, AL548672, BC001790, BM147696, DN997252
- Consensus CDS
-
CCDS81655.1
- UniProtKB/Swiss-Prot
- Q0D2I5, Q24JT6, Q7L5J9, Q7Z5X4, Q9BQ46
- Related
- ENSP00000380052.2, ENST00000396840.6
-
NM_001330325.2 → NP_001317254.1 non-homologous end joining factor IFFO1 isoform 8
Status: REVIEWED
- Description
- Transcript Variant: This variant (9) uses an alternate in-frame splice site in the central coding region, compared to variant 2, resulting in an isoform (8) that is 1 aa shorter than isoform 2.
- Source sequence(s)
-
AA251428, AC006064, AF124432, AL548672, BC001790, BE410988, BM147696
- Conserved Domains (1) summary
-
- pfam00038
Location:230 → 520
- Filament; Intermediate filament protein
-
NM_080730.5 → NP_542768.2 non-homologous end joining factor IFFO1 isoform 2
See identical proteins and their annotated locations for NP_542768.2
Status: REVIEWED
- Description
- Transcript Variant: This variant (2) encodes isoform 2.
- Source sequence(s)
-
AA251428, AC006064, AF124432, AL548672, BC001790, BM147696
- Consensus CDS
-
CCDS8550.2
- UniProtKB/Swiss-Prot
-
Q0D2I5
- Related
- ENSP00000337593.4, ENST00000336604.8
- Conserved Domains (1) summary
-
- pfam00038
Location:230 → 521
- Filament; Intermediate filament protein
RNA
-
NR_036467.2 RNA Sequence
Status: REVIEWED
- Description
- Transcript Variant: This variant (7) includes an additional internal exon in the 5' region and uses an alternate splice site in the central region, compared to variant 2. This variant is represented as non-coding because the use of the supported translational start codon, as used in variant 2, renders the transcript a candidate for nonsense-mediated mRNA decay (NMD).
- Source sequence(s)
-
AA251428, AC006064, BC001790
- Related
-
ENST00000487279.6
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_001193459.1: Suppressed sequence
- Description
- NM_001193459.1: This RefSeq was permanently suppressed because currently there is support for the transcript but not for the protein.
-
NM_015438.1: Suppressed sequence
- Description
- NM_015438.1: This RefSeq was permanently suppressed because it is a nonsense-mediated mRNA decay (NMD) candidate.
-
NM_080731.3: Suppressed sequence
- Description
- NM_080731.3: This RefSeq was permanently suppressed because currently there is support for the transcript but not for the protein.