Human (GRCh38.p14)
Description

synapsin I [Source:HGNC Symbol;Acc:HGNC:11494]

Gene Synonyms

MRX50

Location
About this transcript

This transcript has 13 exons, is annotated with 38 domains and features, is associated with 14995 variant alleles and maps to 581 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000295987.13SYN1-2013210705aaENSP00000295987.7
 
Protein coding
CCDS14280P17600-1 NM_006950.3MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P3TSL:2
ENST00000340666.5SYN1-2023172669aaENSP00000343206.4
 
Protein coding
CCDS35233P17600-2 -GENCODE basicAPPRIS ALT1TSL:1
ENST00000640721.1SYN1-20572555aaENSP00000492857.1
 
Protein coding
A0A1W2PSE9 -TSL:5CDS 5' incomplete
ENST00000639776.1SYN1-204688148aaENSP00000492521.1
 
Protein coding
A0A1W2PS00 -TSL:3CDS 5' incomplete
ENST00000638337.1SYN1-203585No protein-
 
Retained intron
--TSL:2
Statistics

Exons: 13, Coding exons: 13, Transcript length: 3,210 bps, Translation length: 705 residues

MANE

This MANE Select transcript contains ENSP00000295987 and matches to NM_006950.3 and NP_008881.2

Uniprot

This transcript corresponds to the following Uniprot identifiers: P17600

CCDS

This transcript is a member of the Human CCDS set: CCDS14280

Transcript Support Level (TSL)

TSL:2

Version

ENST00000295987.13

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.

Annotation Attributes

not organism-supported [Definitions]

GENCODE basic gene

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