Transcript: ENST00000298139.5 WRN-001

Description

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

Gene Synonyms

RECQ3, RECQL2, RECQL3

Location

About this transcript

This transcript has 35 exons, is annotated with 31 domains and features, is associated with 59490 variant alleles and maps to 933 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: 35, Coding exons: 34, Transcript length: 5,215 bps, Translation length: 1,432 residues

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q14191

CCDS

This transcript is a member of the Human CCDS set: CCDS6082

Version

ENST00000298139.5

Type

Protein coding

Annotation Method

Transcript where the Ensembl genebuild transcript and the Havana manual annotation have the same sequence, for every base pair. See article.

Alternative transcripts

This transcript corresponds to the following database identifiers:

Transcript having exact match between ENSEMBL and HAVANA:	OTTHUMT00000376248 (version 1)

GENCODE basic gene

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