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 11 domains and features, is associated with 2613 variant alleles and maps to 199 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: 4,594 bps, Translation length: 248 residues

MANE

This MANE Select transcript contains ENSP00000348998 and matches to NM_030817.3 and NP_110444.3

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q96LR9

CCDS

This transcript is a member of the Human CCDS set: CCDS8654

Transcript Support Level (TSL)

TSL:1

Version

ENST00000356591.5

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.