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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_001024385.1 → NP_001019556.1 cardiolipin synthase (CMP-forming) isoform 1
See identical proteins and their annotated locations for NP_001019556.1
Status: VALIDATED
- Description
- Transcript Variant: This variant (1) encodes the longer isoform (1).
- Source sequence(s)
-
AK018180, BC048702, BC086619
- Consensus CDS
-
CCDS16779.1
- UniProtKB/Swiss-Prot
- Q80ZM8, Q9D4U1
- Related
- ENSMUSP00000028835.7, ENSMUST00000028835.13
- Conserved Domains (1) summary
-
- COG0558
Location:108 → 298
- PgsA; Phosphatidylglycerophosphate synthase [Lipid transport and metabolism]
-
NM_025646.3 → NP_079922.2 cardiolipin synthase (CMP-forming) isoform 2
See identical proteins and their annotated locations for NP_079922.2
Status: VALIDATED
- Description
- Transcript Variant: This variant (2) has an alternate 5' exon and the translation initiates from a downstream AUG codon, as compared to variant 1. The encoded isoform 2 has a shorter N-terminus, as compared to isoform 1.
- Source sequence(s)
-
AK016165, BC086619
- Consensus CDS
-
CCDS38247.1
- UniProtKB/TrEMBL
- A0A0C3SFZ5, E9PYF8
- Related
- ENSMUSP00000132682.2, ENSMUST00000124836.8
- Conserved Domains (1) summary
-
- PLN02794
Location:1 → 174
- PLN02794; cardiolipin synthase
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_001024384.1: Suppressed sequence
- Description
- NM_001024384.1: This RefSeq was permanently suppressed because it is a nonsense-mediated mRNA decay (NMD) candidate.