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Human (GRCh38.p14)
Description

NHS like 3 [Source:HGNC Symbol;Acc:HGNC:29301]

Gene Synonyms

KIAA1522

Location
About this transcript

This transcript has 7 exons, is annotated with 48 domains and features, is associated with 15612 variant alleles and maps to 385 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000401073.7NHSL3-20454931094aaENSP00000383851.2
 
Protein coding
CCDS41298Q9P206-2 NM_020888.3MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS ALT2TSL:2
ENST00000373480.1NHSL3-20252941035aaENSP00000362579.1
 
Protein coding
CCDS55588Q9P206-1 -GENCODE PrimaryGENCODE BasicAPPRIS P2TSL:1
ENST00000373481.7NHSL3-20352931046aaENSP00000362580.3
 
Protein coding
CCDS90910Q9P206-3 -GENCODE PrimaryGENCODE BasicAPPRIS ALT2TSL:2
ENST00000294521.7NHSL3-201878143aaENSP00000294521.3
 
Protein coding
CCDS55589Q9P206-4 -GENCODE PrimaryGENCODE BasicAPPRIS ALT2TSL:2
ENST00000468130.1NHSL3-205684No protein-
 
Retained intron
--TSL:2
Statistics

Exons: 7, Coding exons: 7, Transcript length: 5,493 bps, Translation length: 1,094 residues

MANE

This MANE Select transcript contains ENSP00000383851 and matches to NM_020888.3 and NP_065939.2

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q9P206

CCDS

This transcript is a member of the Human CCDS set: CCDS41298

Transcript Support Level (TSL)

TSL:2

Version

ENST00000401073.7

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.