Canonical Allele Identifier: CA1402648419

Gene: NPHP3 NPHP3-ACAD11

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.132684785G= , CM000665.2:g.132684785G=	GRCh38
NC_000003.11:g.132403629G= , CM000665.1:g.132403629G=	GRCh37
NC_000003.10:g.133886319G=	NCBI36
NG_008130.1:g.42648C=
NG_008130.2:g.42648C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000684294.1:c.*1247C= (NPHP3)	ENSP00000508078.1:n.*1247C=
ENST00000337331.10:c.3339C= (NPHP3) MANE Select	ENSP00000338766.5:p.Asp1113=
ENST00000337331.9:c.3339C= (NPHP3)	ENSP00000338766.5:p.Asp1113=
ENST00000465756.5:c.*1247C= (NPHP3)	ENSP00000419907.1:n.*1247C=
ENST00000471702.2:c.*1330C= (NPHP3-ACAD11)	ENSP00000419763.1:n.*1330C=
ENST00000474871.5:n.2538C= (NPHP3)
ENST00000490993.5:n.4064C= (NPHP3)
ENST00000493732.5:n.39C= (NPHP3)
NM_153240.4:c.3339C= (NPHP3)	NP_694972.3:p.Asp1113=
NR_037804.1:n.3345C= (NPHP3-ACAD11)
NM_153240.5:c.3339C= (NPHP3) MANE Select	NP_694972.3:p.Asp1113=