Canonical Allele Identifier: CA16609833
Gene: NPHP3 HGNC NCBI
NPHP3-ACAD11 HGNC NCBI

Linked Data

ClinVar Variation Id: 403710
ClinVar RCV Id: RCV000456125
dbSNP Id: rs1060499938

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.132683487del , CM000665.2:g.132683487del GRCh38
NC_000003.11:g.132402331del , CM000665.1:g.132402331del GRCh37
NC_000003.10:g.133885021del NCBI36
NG_008130.1:g.43946del
NG_008130.2:g.43946del

Transcript Alleles

HGVS Amino-acid change
ENST00000684294.1:c.*1536del (NPHP3) ENSP00000508078.1:n.*1536del
ENST00000337331.10:c.3608del (NPHP3) MANE Select ENSP00000338766.5:p.Ala1203ValfsTer16
ENST00000337331.9:c.3608del (NPHP3) ENSP00000338766.5:p.Ala1203ValfsTer16
ENST00000465756.5:c.*1516del (NPHP3) ENSP00000419907.1:n.*1516del
ENST00000471702.2:c.*1599del (NPHP3-ACAD11) ENSP00000419763.1:n.*1599del
ENST00000474871.5:n.2807del (NPHP3)
ENST00000490993.5:n.4333del (NPHP3)
ENST00000493732.5:n.308del (NPHP3)
ENST00000512094.5:c.170del (NPHP3) ENSP00000427666.1:p.Ala57ValfsTer16
ENST00000632629.1:c.255del (NPHP3-ACAD11)
NM_153240.4:c.3608del (NPHP3) NP_694972.3:p.Ala1203ValfsTer16
NR_037804.1:n.3614del (NPHP3-ACAD11)
NM_153240.5:c.3608del (NPHP3) MANE Select NP_694972.3:p.Ala1203ValfsTer16