Canonical Allele Identifier: CA354579116

Gene: NPHP3 NPHP3-ACAD11

Linked Data

• MyVariant Identifiers: chr3:g.132403578A>C (hg19) ; chr3:g.132684734A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.132684734A>C , CM000665.2:g.132684734A>C	GRCh38
NC_000003.11:g.132403578A>C , CM000665.1:g.132403578A>C	GRCh37
NC_000003.10:g.133886268A>C	NCBI36
NG_008130.1:g.42699T>G
NG_008130.2:g.42699T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684294.1:c.*1298T>G (NPHP3)	ENSP00000508078.1:n.*1298T>G
ENST00000337331.10:c.3390T>G (NPHP3) MANE Select	ENSP00000338766.5:p.Asp1130Glu
ENST00000337331.9:c.3390T>G (NPHP3)	ENSP00000338766.5:p.Asp1130Glu
ENST00000465756.5:c.*1298T>G (NPHP3)	ENSP00000419907.1:n.*1298T>G
ENST00000471702.2:c.*1381T>G (NPHP3-ACAD11)	ENSP00000419763.1:n.*1381T>G
ENST00000474871.5:n.2589T>G (NPHP3)
ENST00000490993.5:n.4115T>G (NPHP3)
ENST00000493732.5:n.90T>G (NPHP3)
ENST00000632629.1:c.37T>G (NPHP3-ACAD11)
NM_153240.4:c.3390T>G (NPHP3)	NP_694972.3:p.Asp1130Glu
NR_037804.1:n.3396T>G (NPHP3-ACAD11)
NM_153240.5:c.3390T>G (NPHP3) MANE Select	NP_694972.3:p.Asp1130Glu