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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_001286550.2 → NP_001273479.1 colipase-like protein 2 isoform a
Status: VALIDATED
- Description
- Transcript Variant: This variant (1) encodes the longer isoform (a).
- Source sequence(s)
-
AL157823, AY358823, CD513822
- Consensus CDS
-
CCDS69095.1
- UniProtKB/Swiss-Prot
-
Q6UWE3
- Related
- ENSP00000353639.2, ENST00000360454.6
- Conserved Domains (1) summary
-
- cl24053
Location:33 → 69
- COLIPASE; Colipase; a stoichiometric cofactor for pancreatic lipase, allowing the enzyme to anchor itself to the water-lipid interface and stabilizing the active enzyme conformation
-
NM_207409.4 → NP_997292.2 colipase-like protein 2 isoform b precursor
See identical proteins and their annotated locations for NP_997292.2
Status: VALIDATED
- Description
- Transcript Variant: This variant (2) lacks an alternate exon that results in a frameshift in the 3' coding region, compared to variant 1. The encoded isoform (b) has a distinct C-terminus and is shorter than isoform a.
- Source sequence(s)
-
AL157823, AW665167, CD513822
- Consensus CDS
-
CCDS4810.2
- UniProtKB/Swiss-Prot
- B0QZ45, Q5T9G3, Q6UWE3
- Related
- ENSP00000385898.3, ENST00000403376.4
- Conserved Domains (1) summary
-
- cl29842
Location:33 → 100
- COLIPASE; Colipase; a stoichiometric cofactor for pancreatic lipase, allowing the enzyme to anchor itself to the water-lipid interface and stabilizing the active enzyme conformation
RNA
-
NR_104467.2 RNA Sequence
Status: VALIDATED
- Description
- Transcript Variant: This variant (3) uses an alternate splice site in the 5' terminal exon and lacks an internal exon, 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)
-
AL157823, CD513822
- Related
-
ENST00000481904.5
-
NR_104469.2 RNA Sequence
Status: VALIDATED
- Description
- Transcript Variant: This variant (4) uses an alternate splice site in the 5' terminal exon and lacks two internal exons, compared to variant 1. This variant is represented as non-coding because the predicted protein does not meet RefSeq quality criteria.
- Source sequence(s)
-
AA861820, AL157823, CD513822
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_000006.12 Reference GRCh38.p14 Primary Assembly
- Range
-
35776598..35779552
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)
Alternate T2T-CHM13v2.0
Genomic
-
NC_060930.1 Alternate T2T-CHM13v2.0
- Range
-
35596952..35599906
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)