Canonical Allele Identifier: CA1402652000

Gene: NPHP3 NPHP3-ACAD11

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.132689151C= , CM000665.2:g.132689151C=	GRCh38
NC_000003.11:g.132407995C= , CM000665.1:g.132407995C=	GRCh37
NC_000003.10:g.133890685C=	NCBI36
NG_008130.1:g.38282G=
NG_008130.2:g.38282G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684294.1:c.*714G= (NPHP3)	ENSP00000508078.1:n.*714G=
ENST00000337331.10:c.2806G= (NPHP3) MANE Select	ENSP00000338766.5:p.Glu936=
ENST00000337331.9:c.2806G= (NPHP3)	ENSP00000338766.5:p.Glu936=
ENST00000465756.5:c.*714G= (NPHP3)	ENSP00000419907.1:n.*714G=
ENST00000471702.2:c.*797G= (NPHP3-ACAD11)	ENSP00000419763.1:n.*797G=
ENST00000474871.5:n.540G= (NPHP3)
ENST00000490993.5:n.3531G= (NPHP3)
NM_153240.4:c.2806G= (NPHP3)	NP_694972.3:p.Glu936=
NR_037804.1:n.2812G= (NPHP3-ACAD11)
NM_153240.5:c.2806G= (NPHP3) MANE Select	NP_694972.3:p.Glu936=