Canonical Allele Identifier: CA1402645468
Gene: NPHP3 HGNC NCBI
NPHP3-ACAD11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.132681989C= , CM000665.2:g.132681989C= GRCh38
NC_000003.11:g.132400833C= , CM000665.1:g.132400833C= GRCh37
NC_000003.10:g.133883523C= NCBI36
NG_008130.1:g.45444G=
NG_008130.2:g.45444G=

Transcript Alleles

HGVS Amino-acid change
ENST00000684294.1:c.*1842G= (NPHP3) ENSP00000508078.1:n.*1842G=
ENST00000337331.10:c.3914G= (NPHP3) MANE Select ENSP00000338766.5:p.Arg1305=
ENST00000337331.9:c.3914G= (NPHP3) ENSP00000338766.5:p.Arg1305=
ENST00000465756.5:c.*1822G= (NPHP3) ENSP00000419907.1:n.*1822G=
ENST00000471702.2:c.*1905G= (NPHP3-ACAD11) ENSP00000419763.1:n.*1905G=
ENST00000474871.5:n.3113G= (NPHP3)
ENST00000490993.5:n.4639G= (NPHP3)
ENST00000493732.5:n.1226G= (NPHP3)
ENST00000512094.5:c.360G= (NPHP3) ENSP00000427666.1:n.360G=
ENST00000632629.1:c.561G= (NPHP3-ACAD11)
NM_153240.4:c.3914G= (NPHP3) NP_694972.3:p.Arg1305=
NR_037804.1:n.3920G= (NPHP3-ACAD11)
NM_153240.5:c.3914G= (NPHP3) MANE Select NP_694972.3:p.Arg1305=