Human (GRCh38.p14)
Description

family with sequence similarity 171 member A2 [Source:HGNC Symbol;Acc:HGNC:30480]

Gene Synonyms

MGC34829

Location
About this transcript

This transcript has 8 exons, is annotated with 27 domains and features, is associated with 5115 variant alleles and maps to 376 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000293443.12FAM171A2-2013138826aaENSP00000293443.6
 
Protein coding
CCDS45701A8MVW0 NM_198475.3MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000589407.5FAM171A2-2031066159aaENSP00000466195.1
 
Nonsense mediated decay
K7EMG4 -TSL:3
ENST00000588067.1FAM171A2-202964159aaENSP00000466493.1
 
Nonsense mediated decay
K7EMG4 -TSL:5
ENST00000592560.1FAM171A2-204758No protein-
 
Retained intron
--TSL:2
Statistics

Exons: 8, Coding exons: 8, Transcript length: 3,138 bps, Translation length: 826 residues

MANE

This MANE Select transcript contains ENSP00000293443 and matches to NM_198475.3 and NP_940877.2

Uniprot

This transcript corresponds to the following Uniprot identifiers: A8MVW0

CCDS

This transcript is a member of the Human CCDS set: CCDS45701

Transcript Support Level (TSL)

TSL:1

Version

ENST00000293443.12

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.