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Human (GRCh37.p13)
Description

Usher syndrome 2A (autosomal recessive, mild) [Source:HGNC Symbol;Acc:12601]

Gene Synonyms

RP39, US2, USH2, dJ1111A8.1

About this transcript

This transcript has 4 exons, is associated with 1797 variant alleles and maps to 85 oligo probes.

Gene
NameTranscript IDbpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
USH2A-002ENST00000307340.3188835202aaENSP00000305941.3
 
Protein coding
CCDS31025O75445 NM_206933
NP_996816
GENCODE basic
USH2A-001ENST00000366942.363201546aaENSP00000355909.3
 
Protein coding
CCDS1516O75445 NM_007123
NP_009054
GENCODE basic
USH2A-201ENST00000366943.2189555226aaENSP00000355910.2
 
Protein coding
-O75445 -GENCODE basic
USH2A-003ENST00000481786.1626No protein-
 
Retained intron
----
USH2A-004ENST00000463147.1618No protein-
 
Retained intron
----
Statistics

Exons: 4, Coding exons: 0, Transcript length: 626 bps,

Incomplete CDS

CDS 5' and 3' incomplete

Version

ENST00000481786.1

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:
OTTHUMT00000089986 (version 3)

Transcript-based displays