Human (GRCh38.p14)
Description

apolipoprotein L domain containing 1 [Source:HGNC Symbol;Acc:HGNC:25268]

Gene Synonyms

DKFZP434F0318, FLJ25138

Location
About this transcript

This transcript has 2 exons, is annotated with 12 domains and features, is associated with 28821 variant alleles and maps to 232 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000356591.5APOLD1-2024594248aaENSP00000348998.4
 
Protein coding
CCDS8654Q96LR9-2 NM_030817.3MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000326765.10APOLD1-2014724279aaENSP00000324277.6
 
Protein coding
CCDS44833Q96LR9-1 -GENCODE basicTSL:1
ENST00000534843.1APOLD1-203237540aaENSP00000456719.1
 
Nonsense mediated decay
F5GX34 -TSL:2
ENST00000540583.5APOLD1-20457440aaENSP00000454511.1
 
Nonsense mediated decay
F5GX34 -TSL:4
ENST00000588943.1APOLD1-205461No protein-
 
Retained intron
--TSL:4
Statistics

Exons: 2, Coding exons: 2, Transcript length: 4,724 bps, Translation length: 279 residues

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q96LR9

CCDS

This transcript is a member of the Human CCDS set: CCDS44833

Transcript Support Level (TSL)

TSL:1

Version

ENST00000326765.10

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.