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Human (GRCh38.p14)
Description

family with sequence similarity 50 member A [Source:HGNC Symbol;Acc:HGNC:18786]

Gene Synonyms

9F, DXS9928E, HXC-26, XAP5

About this transcript

This transcript has 13 exons, is annotated with 16 domains and features, is associated with 2583 variant alleles and maps to 529 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000393600.8FAM50A-2021337339aaENSP00000377225.3
 
Protein coding
CCDS14751Q14320 NM_004699.4MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS P1TSL:1
ENST00000158526.9FAM50A-2011240260aaENSP00000158526.9
 
Protein coding
B0S8I6 -TSL:5CDS 3' incomplete
ENST00000464419.5FAM50A-2031470No protein-
 
Retained intron
--TSL:5
ENST00000481619.5FAM50A-205763No protein-
 
Retained intron
--TSL:2
ENST00000478509.1FAM50A-204682No protein-
 
Retained intron
--TSL:3
ENST00000490480.1FAM50A-206346No protein-
 
Retained intron
--TSL:5
ENST00000494278.1FAM50A-207294No protein-
 
Retained intron
--TSL:2
Statistics

Exons: 13, Coding exons: 13, Transcript length: 1,337 bps, Translation length: 339 residues

MANE

This MANE Select transcript contains ENSP00000377225 and matches to NM_004699.4 and NP_004690.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q14320

CCDS

This transcript is a member of the Human CCDS set: CCDS14751

Transcript Support Level (TSL)

TSL:1

Version

ENST00000393600.8

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.