Human (GRCh38.p14)
Description

deleted in lymphocytic leukemia 7 [Source:HGNC Symbol;Acc:HGNC:17567]

Gene Synonyms

FLJ44882

Location
About this transcript

This transcript has 2 exons, is annotated with 7 domains and features, is associated with 7938 variant alleles and maps to 177 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000504404.2DLEU7-2041121221aaENSP00000427177.1
 
Protein coding
CCDS76635Q6UYE1-1 NM_001306135.2MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000400393.3DLEU7-2012092160aaENSP00000420976.1
 
Protein coding
CCDS53869Q6UYE1-2 -GENCODE basicTSL:1
ENST00000651397.1DLEU7-2063162153aaENSP00000516015.1
 
Nonsense mediated decay
A0A994J5B2 -CDS 5' incomplete
ENST00000651265.1DLEU7-205150033aaENSP00000516017.1
 
Nonsense mediated decay
A0A994J7M1 -CDS 5' incomplete
ENST00000443723.1DLEU7-2032291No protein-
 
Protein coding CDS not defined
--TSL:2
ENST00000428276.1DLEU7-202731No protein-
 
Protein coding CDS not defined
--TSL:3
Statistics

Exons: 2, Coding exons: 2, Transcript length: 1,121 bps, Translation length: 221 residues

MANE

This MANE Select transcript contains ENSP00000427177 and matches to NM_001306135.2 and NP_001293064.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q6UYE1

CCDS

This transcript is a member of the Human CCDS set: CCDS76635

Transcript Support Level (TSL)

TSL:1

Version

ENST00000504404.2

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.