Canonical Allele Identifier: CA1402645483
Gene: NPHP3 HGNC NCBI
NPHP3-ACAD11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.132681991T= , CM000665.2:g.132681991T= GRCh38
NC_000003.11:g.132400835T= , CM000665.1:g.132400835T= GRCh37
NC_000003.10:g.133883525T= NCBI36
NG_008130.1:g.45442A=
NG_008130.2:g.45442A=

Transcript Alleles

HGVS Amino-acid change
ENST00000684294.1:c.*1840A= (NPHP3) ENSP00000508078.1:n.*1840A=
ENST00000337331.10:c.3912A= (NPHP3) MANE Select ENSP00000338766.5:p.Ser1304=
ENST00000337331.9:c.3912A= (NPHP3) ENSP00000338766.5:p.Ser1304=
ENST00000465756.5:c.*1820A= (NPHP3) ENSP00000419907.1:n.*1820A=
ENST00000471702.2:c.*1903A= (NPHP3-ACAD11) ENSP00000419763.1:n.*1903A=
ENST00000474871.5:n.3111A= (NPHP3)
ENST00000490993.5:n.4637A= (NPHP3)
ENST00000493732.5:n.1224A= (NPHP3)
ENST00000512094.5:c.358A= (NPHP3) ENSP00000427666.1:n.358A=
ENST00000632629.1:c.559A= (NPHP3-ACAD11)
NM_153240.4:c.3912A= (NPHP3) NP_694972.3:p.Ser1304=
NR_037804.1:n.3918A= (NPHP3-ACAD11)
NM_153240.5:c.3912A= (NPHP3) MANE Select NP_694972.3:p.Ser1304=