Canonical Allele Identifier: CA1402637751

Gene: NPHP3 NPHP3-ACAD11

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.132700341G= , CM000665.2:g.132700341G=	GRCh38
NC_000003.11:g.132419185G= , CM000665.1:g.132419185G=	GRCh37
NC_000003.10:g.133901875G=	NCBI36
NG_008130.1:g.27092C=
NG_008130.2:g.27092C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684294.1:c.1442C= (NPHP3)	ENSP00000508078.1:p.Thr481=
ENST00000337331.10:c.1736C= (NPHP3) MANE Select	ENSP00000338766.5:p.Thr579=
ENST00000337331.9:c.1736C= (NPHP3)	ENSP00000338766.5:p.Thr579=
ENST00000465756.5:c.1442C= (NPHP3)	ENSP00000419907.1:p.Thr481=
ENST00000469232.5:c.1551C= (NPHP3)	ENSP00000418664.1:n.1551C=
ENST00000471702.2:c.1736C= (NPHP3-ACAD11)	ENSP00000419763.1:p.Thr579=
ENST00000490993.5:n.1512C= (NPHP3)
NM_153240.4:c.1736C= (NPHP3)	NP_694972.3:p.Thr579=
NR_037804.1:n.1840C= (NPHP3-ACAD11)
NM_153240.5:c.1736C= (NPHP3) MANE Select	NP_694972.3:p.Thr579=