Canonical Allele Identifier: CA2667739604
Gene: NPHP3 HGNC NCBI
NPHP3-ACAD11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.132700408_132700410del , CM000665.2:g.132700408_132700410del GRCh38
NC_000003.11:g.132419252_132419254del , CM000665.1:g.132419252_132419254del GRCh37
NC_000003.10:g.133901942_133901944del NCBI36
NG_008130.1:g.27025_27027del
NG_008130.2:g.27025_27027del

Transcript Alleles

HGVS Amino-acid Change
ENST00000684294.1:c.1375_1377del (NPHP3) ENSP00000508078.1:p.Leu459del
ENST00000337331.10:c.1669_1671del (NPHP3) MANE Select ENSP00000338766.5:p.Leu557del
ENST00000337331.9:c.1669_1671del (NPHP3) ENSP00000338766.5:p.Leu557del
ENST00000465756.5:c.1375_1377del (NPHP3) ENSP00000419907.1:p.Leu459del
ENST00000469232.5:c.1484_1486del (NPHP3) ENSP00000418664.1:n.1484_1486del
ENST00000471702.2:c.1669_1671del (NPHP3-ACAD11) ENSP00000419763.1:p.Leu557del
ENST00000490993.5:n.1445_1447del (NPHP3)
NM_153240.4:c.1669_1671del (NPHP3) NP_694972.3:p.Leu557del
NR_037804.1:n.1773_1775del (NPHP3-ACAD11)
NM_153240.5:c.1669_1671del (NPHP3) MANE Select NP_694972.3:p.Leu557del