Canonical Allele Identifier: CA1402645490

Gene: NPHP3 NPHP3-ACAD11

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.132681996G= , CM000665.2:g.132681996G=	GRCh38
NC_000003.11:g.132400840G= , CM000665.1:g.132400840G=	GRCh37
NC_000003.10:g.133883530G=	NCBI36
NG_008130.1:g.45437C=
NG_008130.2:g.45437C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000684294.1:c.*1835C= (NPHP3)	ENSP00000508078.1:n.*1835C=
ENST00000337331.10:c.3907C= (NPHP3) MANE Select	ENSP00000338766.5:p.Pro1303=
ENST00000337331.9:c.3907C= (NPHP3)	ENSP00000338766.5:p.Pro1303=
ENST00000465756.5:c.*1815C= (NPHP3)	ENSP00000419907.1:n.*1815C=
ENST00000471702.2:c.*1898C= (NPHP3-ACAD11)	ENSP00000419763.1:n.*1898C=
ENST00000474871.5:n.3106C= (NPHP3)
ENST00000490993.5:n.4632C= (NPHP3)
ENST00000493732.5:n.1219C= (NPHP3)
ENST00000512094.5:c.353C= (NPHP3)	ENSP00000427666.1:n.353C=
ENST00000632629.1:c.554C= (NPHP3-ACAD11)
NM_153240.4:c.3907C= (NPHP3)	NP_694972.3:p.Pro1303=
NR_037804.1:n.3913C= (NPHP3-ACAD11)
NM_153240.5:c.3907C= (NPHP3) MANE Select	NP_694972.3:p.Pro1303=