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Human (GRCh37.p13)
Description

nephrosis 1, congenital, Finnish type (nephrin) [Source:HGNC Symbol;Acc:7908]

Gene Synonyms

CNF, NPHN, nephrin

Location
About this transcript

This transcript has 4 exons, is associated with 756 variant alleles and maps to 78 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000378910.5NPHS1-00142761241aaENSP00000368190.4
 
Protein coding
CCDS32996O60500 NM_004646.3Ensembl CanonicalGENCODE basic
ENST00000353632.6NPHS1-00237411201aaENSP00000343634.5
 
Protein coding
O60500 -GENCODE basic
ENST00000591817.1NPHS1-005581No protein-
 
Processed transcript
---
ENST00000585400.1NPHS1-003999No protein-
 
Retained intron
---
ENST00000592132.1NPHS1-004561No protein-
 
Retained intron
---
Statistics

Exons: 4, Coding exons: 0, Transcript length: 561 bps,

Version

ENST00000592132.1

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:
OTTHUMT00000452556 (version 1)