Human (GRCh38.p14)
Description

SLAIN motif family member 2 [Source:HGNC Symbol;Acc:HGNC:29282]

Gene Synonyms

FLJ21611, KIAA1458

Location
About this transcript

This transcript has 8 exons, is annotated with 27 domains and features, is associated with 38365 variant alleles and maps to 816 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000264313.11SLAIN2-2016081581aaENSP00000264313.5
 
Protein coding
CCDS47051A0A024R9T6 Q9P270 NM_020846.2MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000512093.5SLAIN2-2054219414aaENSP00000425923.1
 
Protein coding
D6RIF6 -GENCODE basicTSL:5
ENST00000510595.1SLAIN2-204550169aaENSP00000424473.1
 
Protein coding
H0Y9L2 -TSL:4CDS 5' incomplete
ENST00000505131.1SLAIN2-20258858aaENSP00000426744.1
 
Nonsense mediated decay
D6REM5 -TSL:4
ENST00000506375.1SLAIN2-203349No protein-
 
Protein coding CDS not defined
--TSL:5
Statistics

Exons: 8, Coding exons: 8, Transcript length: 6,081 bps, Translation length: 581 residues

MANE

This MANE Select transcript contains ENSP00000264313 and matches to NM_020846.2 and NP_065897.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q9P270

CCDS

This transcript is a member of the Human CCDS set: CCDS47051

Transcript Support Level (TSL)

TSL:1

Version

ENST00000264313.11

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.