Human (GRCh38.p14)
Description

calsequestrin 2 [Source:HGNC Symbol;Acc:HGNC:1513]

Gene Synonyms

PDIB2

About this transcript

This transcript has 11 exons, is annotated with 49 domains and features, is associated with 32018 variant alleles and maps to 468 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000261448.6CASQ2-2012593399aaENSP00000261448.5
 
Protein coding
CCDS884O14958-1 NM_001232.4MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS P1TSL:1
ENST00000713711.1CASQ2-2034717446aaENSP00000519014.1
 
Protein coding
--GENCODE PrimaryGENCODE Basic
ENST00000850611.1CASQ2-2092750189aaENSP00000520899.1
 
Protein coding
--GENCODE PrimaryGENCODE Basic
ENST00000713728.1CASQ2-2072630307aaENSP00000519032.1
 
Protein coding
--GENCODE Basic
ENST00000713713.1CASQ2-2051173252aaENSP00000519016.1
 
Protein coding
--GENCODE Basic
ENST00000713727.1CASQ2-2064984300aaENSP00000519031.1
 
Nonsense mediated decay
---
ENST00000713729.1CASQ2-2083045323aaENSP00000519033.1
 
Nonsense mediated decay
---
ENST00000488931.2CASQ2-2022511148aaENSP00000518226.1
 
Nonsense mediated decay
A0AA34QVH1 -TSL:3
ENST00000713712.1CASQ2-204225148aaENSP00000519015.1
 
Nonsense mediated decay
---
ENST00000850612.1CASQ2-2104964No protein-
 
Protein coding CDS not defined
---
Statistics

Exons: 11, Coding exons: 11, Transcript length: 2,593 bps, Translation length: 399 residues

MANE

This MANE Select transcript contains ENSP00000261448 and matches to NM_001232.4 and NP_001223.2

Uniprot

This transcript corresponds to the following Uniprot identifiers: O14958

CCDS

This transcript is a member of the Human CCDS set: CCDS884

Transcript Support Level (TSL)

TSL:1

Version

ENST00000261448.6

Type

Protein coding

Annotation Method

Transcript where the Ensembl genebuild transcript and the Havana manual annotation have the same sequence, for every base pair. See article.

GENCODE basic gene

This transcript is a member of the Gencode basic gene set.

GENCODE primary gene

This transcript is a member of the Gencode Primary gene set.