Human (GRCh38.p14)
Description

empty spiracles homeobox 1 [Source:HGNC Symbol;Acc:HGNC:3340]

Location
About this transcript

This transcript has 1 exon, is associated with 1155 variant alleles and maps to 222 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000258106.11EMX1-2012144290aaENSP00000258106.6
 
Protein coding
CCDS1921Q04741-1 NM_004097.3MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000394111.6EMX1-2021528209aaENSP00000482619.1
 
Protein coding
A0A087WZF2 -GENCODE basicTSL:3
ENST00000473732.1EMX1-204480147aaENSP00000446992.1
 
Protein coding
F8W1B5 -TSL:3CDS 3' incomplete
ENST00000491023.3EMX1-2051071No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000616281.1EMX1-2062900No protein-
 
Retained intron
--TSL:NA
ENST00000464675.2EMX1-203959No protein-
 
Retained intron
--TSL:4
Statistics

Exons: 1, Coding exons: 0, Transcript length: 2,900 bps,

Transcript Support Level (TSL)

TSL:NA

Version

ENST00000616281.1

Type

Retained intron

Annotation Method

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