nephrosis 1, congenital, Finnish type (nephrin) [Source:HGNC Symbol;Acc:7908]
CNF, NPHN, nephrin
Chromosome 19: 36,334,400-36,336,412 reverse strand.
This transcript has 3 exons, is associated with 1180 variant alleles and maps to 76 oligo probes.
This transcript is a product of gene ENSG00000161270.15 Show transcript tableHide transcript table
Transcript ID | Name | bp | Protein | Translation ID | Biotype | CCDS | UniProt Match | RefSeq | Flags |
---|---|---|---|---|---|---|---|---|---|
ENST00000378910.5 | NPHS1-001 | 4276 | 1241aa | ENSP00000368190.4 | Protein coding | CCDS32996 | O60500 | NM_004646.3 | GENCODE basic, |
ENST00000353632.6 | NPHS1-002 | 3741 | 1201aa | ENSP00000343634.5 | Protein coding | O60500 | - | GENCODE basic, | |
ENST00000591817.1 | NPHS1-005 | 581 | No protein | - | Processed transcript | - | - | - | |
ENST00000585400.1 | NPHS1-003 | 999 | No protein | - | Retained intron | - | - | - | |
ENST00000592132.1 | NPHS1-004 | 561 | No protein | - | Retained intron | - | - | - |