Human (GRCh38.p14)
Description

SHC binding and spindle associated 1 [Source:HGNC Symbol;Acc:HGNC:29547]

Gene Synonyms

FLJ22009, PAL

Location
About this transcript

This transcript has 13 exons, is annotated with 13 domains and features, is associated with 17339 variant alleles and maps to 529 oligo probes.

Gene
Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000303383.8SHCBP1-2015177672aaENSP00000306473.3
 
Protein coding
CCDS10720Q8NEM2 NM_024745.5MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000569702.1SHCBP1-207465155aaENSP00000460840.1
 
Protein coding
I3L3Z1 -TSL:3CDS 5' and 3' incomplete
ENST00000564272.1SHCBP1-203530No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000566016.5SHCBP1-2051482No protein-
 
Retained intron
--TSL:1
ENST00000565887.1SHCBP1-204603No protein-
 
Retained intron
--TSL:5
ENST00000567698.1SHCBP1-206535No protein-
 
Retained intron
--TSL:2
ENST00000563219.1SHCBP1-202485No protein-
 
Retained intron
--TSL:3
Statistics

Exons: 13, Coding exons: 13, Transcript length: 5,177 bps, Translation length: 672 residues

MANE

This MANE Select transcript contains ENSP00000306473 and matches to NM_024745.5 and NP_079021.4

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q8NEM2

CCDS

This transcript is a member of the Human CCDS set: CCDS10720

Transcript Support Level (TSL)

TSL:1

Version

ENST00000303383.8

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.