Human (GRCh38.p14)
Description

calcium sensing receptor [Source:HGNC Symbol;Acc:HGNC:1514]

Gene Synonyms

FHH, GPRC2A, HHC, HHC1, NSHPT

About this transcript

This transcript has 7 exons, is annotated with 91 domains and features, is associated with 45833 variant alleles and maps to 714 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000639785.2CASR-205100621078aaENSP00000491584.2
 
Protein coding
CCDS3010P41180-1 NM_000388.4MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000638421.1CASR-20450881078aaENSP00000492190.1
 
Protein coding
CCDS3010P41180-1 -GENCODE basicAPPRIS P1TSL:5
ENST00000498619.4CASR-20250091088aaENSP00000420194.1
 
Protein coding
CCDS54632P41180-2 -GENCODE basicTSL:1
ENST00000490131.7CASR-20140151001aaENSP00000418685.2
 
Protein coding
A0A1X7SBX3 -GENCODE basicTSL:5
ENST00000643573.1CASR-2061478No protein-
 
Protein coding CDS not defined
---
ENST00000638296.1CASR-203662No protein-
 
Retained intron
--TSL:2
Statistics

Exons: 7, Coding exons: 6, Transcript length: 10,062 bps, Translation length: 1,078 residues

MANE

This MANE Select transcript contains ENSP00000491584 and matches to NM_000388.4 and NP_000379.3

Uniprot

This transcript corresponds to the following Uniprot identifiers: P41180

CCDS

This transcript is a member of the Human CCDS set: CCDS3010

Transcript Support Level (TSL)

TSL:1

Version

ENST00000639785.2

Type

Protein coding

Annotation Method

Manual annotation (determined on a case-by-case basis) from the Havana project.

GENCODE basic gene

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