Human (GRCh38.p14)
Description

SH2 domain containing 3A [Source:HGNC Symbol;Acc:HGNC:16885]

Gene Synonyms

NSP1

Location
About this transcript

This transcript has 8 exons, is associated with 6794 variant alleles and maps to 353 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000245908.11SH2D3A-2012281576aaENSP00000245908.5
 
Protein coding
CCDS12173Q9BRG2-1 NM_005490.3MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000437152.7SH2D3A-2022013483aaENSP00000393303.2
 
Protein coding
Q9BRG2-2 -GENCODE basicTSL:2
ENST00000597687.1SH2D3A-207859238aaENSP00000470700.1
 
Protein coding
M0QZQ6 -TSL:3CDS 3' incomplete
ENST00000599563.5SH2D3A-208845No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000597254.1SH2D3A-206586No protein-
 
Protein coding CDS not defined
--TSL:4
ENST00000597168.1SH2D3A-205512No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000595369.1SH2D3A-2033493No protein-
 
Retained intron
--TSL:2
ENST00000595681.5SH2D3A-2041750No protein-
 
Retained intron
--TSL:5
Statistics

Exons: 8, Coding exons: 0, Transcript length: 1,750 bps,

Transcript Support Level (TSL)

TSL:5

Version

ENST00000595681.5

Type

Retained intron

Annotation Method

Manual annotation (determined on a case-by-case basis) from the Havana project.