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Human (GRCh38.p14)
Description

notch 2 N-terminal like R [Source:HGNC Symbol;Acc:HGNC:53925]

About this transcript

This transcript has 5 exons, is annotated with 56 domains and features, is associated with 22655 variant alleles and maps to 291 oligo probes.

Gene
Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000624419.3NOTCH2NLR-2012089274aaENSP00000485259.2
 
Protein coding
CCDS91030A0A096LNW5 NM_001396072.1MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicTSL:5
ENST00000690847.1NOTCH2NLR-2021403312aaENSP00000509634.1
 
Protein coding
A0A8I5KY86 -GENCODE PrimaryGENCODE BasicAPPRIS P1
Statistics

Exons: 5, Coding exons: 5, Transcript length: 2,089 bps, Translation length: 274 residues

MANE

This MANE Select transcript contains ENSP00000485259 and matches to NM_001396072.1 and NP_001383001.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: A0A096LNW5

CCDS

This transcript is a member of the Human CCDS set: CCDS91030

Transcript Support Level (TSL)

TSL:5

Version

ENST00000624419.3

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.

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.