Human (GRCh37.p13)
Description

non imprinted in Prader-Willi/Angelman syndrome 1 [Source:HGNC Symbol;Acc:17043]

Gene Synonyms

FSP3, MGC35570, SPG6

Location
About this transcript

This transcript has 2 exons, is associated with 13742 variant alleles and maps to 68 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000437912.2NIPA1-0047613254aaENSP00000393962.2
 
Protein coding
CCDS45190Q3SYP4 Q7RTP0 -GENCODE basic
ENST00000337435.4NIPA1-0016567329aaENSP00000337452.4
 
Protein coding
CCDS10011Q3SYP4 Q7RTP0 NM_144599.4GENCODE basic
ENST00000538684.1NIPA1-2012797159aaENSP00000440957.1
 
Protein coding
Q3SYP4 -GENCODE basic
ENST00000561183.1NIPA1-0031675254aaENSP00000453722.1
 
Protein coding
CCDS45190Q3SYP4 Q7RTP0 -GENCODE basic
ENST00000559448.1NIPA1-002279990aaENSP00000453286.1
 
Nonsense mediated decay
--CDS 5' incomplete
ENST00000557930.1NIPA1-00758258aaENSP00000453797.1
 
Nonsense mediated decay
H0YLJ9 H0YMY7 -CDS 5' incomplete
ENST00000560069.1NIPA1-00857535aaENSP00000453237.1
 
Nonsense mediated decay
H0YLJ9 --
ENST00000560105.1NIPA1-006375No protein-
 
Retained intron
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Statistics

Exons: 2, Coding exons: 0, Transcript length: 375 bps,

Version

ENST00000560105.1

Type

Retained intron

Annotation Method

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

Alternative transcripts

This transcript corresponds to the following database identifiers:

Havana transcript:
OTTHUMT00000415895 (version 1)