Canonical Allele Identifier: CA1402648253
Gene: NPHP3 HGNC NCBI
NPHP3-ACAD11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.132684688T= , CM000665.2:g.132684688T= GRCh38
NC_000003.11:g.132403532T= , CM000665.1:g.132403532T= GRCh37
NC_000003.10:g.133886222T= NCBI36
NG_008130.1:g.42745A=
NG_008130.2:g.42745A=

Transcript Alleles

HGVS Amino-acid change
ENST00000684294.1:c.*1344A= (NPHP3) ENSP00000508078.1:n.*1344A=
ENST00000337331.10:c.3436A= (NPHP3) MANE Select ENSP00000338766.5:p.Asn1146=
ENST00000337331.9:c.3436A= (NPHP3) ENSP00000338766.5:p.Asn1146=
ENST00000465756.5:c.*1344A= (NPHP3) ENSP00000419907.1:n.*1344A=
ENST00000471702.2:c.*1427A= (NPHP3-ACAD11) ENSP00000419763.1:n.*1427A=
ENST00000474871.5:n.2635A= (NPHP3)
ENST00000490993.5:n.4161A= (NPHP3)
ENST00000493732.5:n.136A= (NPHP3)
ENST00000632629.1:c.83A= (NPHP3-ACAD11)
NM_153240.4:c.3436A= (NPHP3) NP_694972.3:p.Asn1146=
NR_037804.1:n.3442A= (NPHP3-ACAD11)
NM_153240.5:c.3436A= (NPHP3) MANE Select NP_694972.3:p.Asn1146=