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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_001277638.2 → NP_001264567.1 chromosome transmission fidelity protein 8 homolog
See identical proteins and their annotated locations for NP_001264567.1
Status: VALIDATED
- Description
- Transcript Variant: This variant (1) is a protein-coding transcript of this gene. Variants 1 and 2 both encode the same protein.
- Source sequence(s)
-
JAENSK010000248
- UniProtKB/TrEMBL
-
F1NU26
- Related
- ENSGALP00010011028.1, ENSGALT00010019480.1
- Conserved Domains (1) summary
-
- pfam09696
Location:19 → 104
- Ctf8; Ctf8
-
NM_001277645.2 → NP_001264574.1 chromosome transmission fidelity protein 8 homolog
See identical proteins and their annotated locations for NP_001264574.1
Status: VALIDATED
- Description
- Transcript Variant: This variant (2) differs in the 5' UTR compared to variant 1. Variants 1 and 2 both encode the same protein.
- Source sequence(s)
-
JAENSK010000248
- UniProtKB/TrEMBL
-
F1NU26
- Conserved Domains (1) summary
-
- pfam09696
Location:19 → 104
- Ctf8; Ctf8
RNA
-
NR_102418.1 RNA Sequence
Status: VALIDATED
- Description
- Transcript Variant: This variant (3) lacks an alternate intron compared to variant 1. This variant is represented as non-coding because the use of the 5'-most expected translational start codon, as used in variant 1, renders the transcript a candidate for nonsense-mediated mRNA decay (NMD).
- Source sequence(s)
-
BU255592, CR352955, CR354334
-
NR_102419.1 RNA Sequence
Status: VALIDATED
- Description
- Transcript Variant: This variant (4) uses an alternate first exon and lacks an alternate intron compared to variant 1. This variant is represented as non-coding because the use of the 5'-most expected translational start codon, as used in variant 1, renders the transcript a candidate for nonsense-mediated mRNA decay (NMD).
- Source sequence(s)
-
CR354334, CR406334