Human (GRCh38.p14)
Description

SNW domain containing 1 [Source:HGNC Symbol;Acc:HGNC:16696]

Gene Synonyms

BX42, FUN20, NCOA-62, PRP45, PRPF45, SKIIP, SKIP, SKIP1

Location
About this transcript

This transcript has 6 exons, is annotated with 5 domains and features, is associated with 12917 variant alleles and maps to 160 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000261531.12SNW1-2012129536aaENSP00000261531.8
 
Protein coding
CCDS9867Q13573 NM_012245.3MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000555761.5SNW1-2051855571aaENSP00000451129.1
 
Protein coding
CCDS81830G3V3A4 -GENCODE basicTSL:2
ENST00000554775.5SNW1-2041687374aaENSP00000452059.1
 
Protein coding
G3V4X8 -GENCODE basicTSL:5
ENST00000554324.1SNW1-203584185aaENSP00000452473.1
 
Protein coding
G3V5R3 -TSL:5CDS 3' incomplete
ENST00000556428.5SNW1-206196647aaENSP00000451741.1
 
Nonsense mediated decay
G3V4E0 -TSL:2
ENST00000557663.1SNW1-207602No protein-
 
Retained intron
--TSL:2
ENST00000553565.1SNW1-202564No protein-
 
Retained intron
--TSL:2
Statistics

Exons: 6, Coding exons: 6, Transcript length: 584 bps, Translation length: 185 residues

Transcript Support Level (TSL)

TSL:5

Incomplete CDS

CDS 3' incomplete

Version

ENST00000554324.1

Type

Protein coding

Annotation Method

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