Transcript: ENST00000520169.1 WRN-003

Description

Werner syndrome, RecQ helicase-like [Source:HGNC Symbol;Acc:12791]

Gene Synonyms

RECQ3, RECQL2, RECQL3

Location

About this transcript

This transcript has 3 exons, is associated with 2264 variant alleles and maps to 80 oligo probes.

Gene

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq	Flags
ENST00000298139.5	WRN-001	5215	1432aa	ENSP00000298139.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS6082	Q14191	NM_000553.4	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENST00000521620.1	WRN-002	3593	No protein	-	An alternatively spliced transcript believed to contain intronic sequence relative to other, coding, transcripts of the same gene.Retained intron		-	-	-
ENST00000520169.1	WRN-003	629	No protein	-	An alternatively spliced transcript believed to contain intronic sequence relative to other, coding, transcripts of the same gene.Retained intron		-	-	-

Summary

Statistics

Exons: 3, Coding exons: 0, Transcript length: 629 bps,

Version

ENST00000520169.1

Type

Retained intron

Annotation Method

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

Alternative transcripts

This transcript corresponds to the following database identifiers:

Havana transcript:	OTTHUMT00000376250 (version 1)