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Human (GRCh37.p13)
Description

non imprinted in Prader-Willi/Angelman syndrome 2 [Source:HGNC Symbol;Acc:17044]

Location
About this transcript

This transcript has 6 exons, is annotated with 18 domains and features, is associated with 16545 variant alleles and maps to 446 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000337451.3NIPA2-0013233360aaENSP00000337618.3
 
Protein coding
CCDS10010H0YMQ7 Q8N8Q9 NM_030922.6Ensembl CanonicalGENCODE basic
ENST00000398014.2NIPA2-2013130360aaENSP00000381096.2
 
Protein coding
CCDS10010H0YMQ7 Q8N8Q9 NM_001008860.2GENCODE basic
ENST00000398013.3NIPA2-0032280360aaENSP00000381095.3
 
Protein coding
CCDS10010H0YMQ7 Q8N8Q9 NM_001008892.2GENCODE basic
ENST00000359727.4NIPA2-0021531341aaENSP00000352762.4
 
Protein coding
CCDS32174Q8N8Q9 NM_001184888.1GENCODE basic
ENST00000539711.2NIPA2-0041412341aaENSP00000437746.2
 
Protein coding
CCDS32174Q8N8Q9 NM_001008894.2GENCODE basic
ENST00000560039.1NIPA2-00955459aaENSP00000453700.1
 
Protein coding
H0YMQ7 -CDS 3' incomplete
ENST00000559571.1NIPA2-007673No protein-
 
Processed transcript
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ENST00000560205.1NIPA2-006589No protein-
 
Processed transcript
---
ENST00000561072.1NIPA2-008574No protein-
 
Processed transcript
---
ENST00000560762.1NIPA2-005534No protein-
 
Processed transcript
---
Statistics

Exons: 6, Coding exons: 5, Transcript length: 2,280 bps, Translation length: 360 residues

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q8N8Q9

CCDS

This transcript is a member of the Human CCDS set: CCDS10010

Version

ENST00000398013.3

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.

Alternative transcripts

This transcript corresponds to the following database identifiers:

Transcript having exact match between ENSEMBL and HAVANA:
OTTHUMT00000415640 (version 1)
GENCODE basic gene

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