Human (GRCh38.p14)
Description

XNDC1N-ZNF705EP-ALG1L9P readthrough [Source:HGNC Symbol;Acc:HGNC:55871]

Location
About this transcript

This transcript has 11 exons, is associated with 62623 variant alleles and maps to 1072 oligo probes.

Gene
Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000696863.1XNDC1N-ZNF705EP-ALG1L9P-2014191269aaENSP00000512936.1
 
Nonsense mediated decay
A0A8Q3WLN7 -Ensembl CanonicalGENCODE basicAPPRIS P5
ENST00000696865.1XNDC1N-ZNF705EP-ALG1L9P-2032665134aaENSP00000512938.1
 
Nonsense mediated decay
E9PLZ0 -APPRIS ALT2
ENST00000696864.1XNDC1N-ZNF705EP-ALG1L9P-2022551196aaENSP00000512937.1
 
Nonsense mediated decay
A0A8Q3WLL2 -APPRIS ALT2
ENST00000696866.1XNDC1N-ZNF705EP-ALG1L9P-204339No protein-
 
Protein coding CDS not defined
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Statistics

Exons: 11, Coding exons: 5, Transcript length: 4,191 bps, Translation length: 269 residues

Version

ENST00000696863.1

Type

Nonsense mediated decay

Annotation Method

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

Annotation Attributes

RNA-Seq supported only [Definitions]

GENCODE basic gene

This transcript is a member of the Gencode basic gene set.