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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 13 exons, is annotated with 11 domains and features, is associated with 19197 variant alleles and maps to 465 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000261531.12SNW1-2012129536aaENSP00000261531.8
 
Protein coding
CCDS9867Q13573 NM_012245.3MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS P1TSL:1
ENST00000555761.5SNW1-2051855571aaENSP00000451129.1
 
Protein coding
CCDS81830G3V3A4 -GENCODE PrimaryGENCODE 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: 13, Coding exons: 13, Transcript length: 1,855 bps, Translation length: 571 residues

CCDS

This transcript is a member of the Human CCDS set: CCDS81830

Transcript Support Level (TSL)

TSL:2

Version

ENST00000555761.5

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.

GENCODE primary gene

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