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 29 exons, is annotated with 63 domains and features, is associated with 14112 variant alleles and maps to 810 oligo probes.

Show/hide columns (1 hidden)
  • Transcript ID
  • Name
  • bp
  • Protein
  • Translation ID
  • Biotype
  • CCDS
  • UniProt Match
  • RefSeq
  • Flags
Transcript IDNamebpProteinBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000378910.5NPHS1-00142761241aa
 
Protein coding
CCDS32996O60500 NM_004646.3Ensembl CanonicalGENCODE Basic
ENST00000353632.6NPHS1-00237411201aa
 
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: 29, Coding exons: 29, Transcript length: 4,276 bps, Translation length: 1,241 residues

Uniprot

This transcript corresponds to the following Uniprot identifiers: O60500

CCDS

This transcript is a member of the Human CCDS set: CCDS32996

Version

ENST00000378910.5

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:
OTTHUMT00000452553 (version 1)
GENCODE basic gene

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