Human (GRCh38.p14)
Description

FPGT-TNNI3K readthrough [Source:HGNC Symbol;Acc:HGNC:42952]

Location
About this transcript

This transcript has 6 exons, is associated with 23192 variant alleles and maps to 121 oligo probes.

Gene
Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000557284.7FPGT-TNNI3K-2062855936aaENSP00000450895.3
 
Protein coding
V9GXZ4 -Ensembl CanonicalGENCODE basicAPPRIS P1TSL:2
ENST00000370895.5FPGT-TNNI3K-2027566697aaENSP00000359932.1
 
Protein coding
--GENCODE basicTSL:2
ENST00000370899.7FPGT-TNNI3K-2032752843aaENSP00000359936.3
 
Protein coding
--GENCODE basicTSL:2
ENST00000370893.1FPGT-TNNI3K-2011195151aaENSP00000359930.1
 
Protein coding
A6NHC7 -GENCODE basicTSL:2
ENST00000534632.5FPGT-TNNI3K-205517162aaENSP00000433587.1
 
Protein coding
E9PKE1 -TSL:4CDS 3' incomplete
ENST00000648585.1FPGT-TNNI3K-2073400183aaENSP00000497631.1
 
Nonsense mediated decay
A0A3B3ITB1 --
ENST00000533006.1FPGT-TNNI3K-204566No protein-
 
Protein coding CDS not defined
--TSL:5
Statistics

Exons: 6, Coding exons: 0, Transcript length: 566 bps,

Transcript Support Level (TSL)

TSL:5

Version

ENST00000533006.1

Type

Protein coding CDS not defined

Annotation Method

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