Canonical Allele Identifier: CA354579027

Gene: NPHP3 NPHP3-ACAD11

Linked Data

• MyVariant Identifiers: chr3:g.132403537A>G (hg19) ; chr3:g.132684693A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.132684693A>G , CM000665.2:g.132684693A>G	GRCh38
NC_000003.11:g.132403537A>G , CM000665.1:g.132403537A>G	GRCh37
NC_000003.10:g.133886227A>G	NCBI36
NG_008130.1:g.42740T>C
NG_008130.2:g.42740T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000684294.1:c.*1339T>C (NPHP3)	ENSP00000508078.1:n.*1339T>C
ENST00000337331.10:c.3431T>C (NPHP3) MANE Select	ENSP00000338766.5:p.Leu1144Pro
ENST00000337331.9:c.3431T>C (NPHP3)	ENSP00000338766.5:p.Leu1144Pro
ENST00000465756.5:c.*1339T>C (NPHP3)	ENSP00000419907.1:n.*1339T>C
ENST00000471702.2:c.*1422T>C (NPHP3-ACAD11)	ENSP00000419763.1:n.*1422T>C
ENST00000474871.5:n.2630T>C (NPHP3)
ENST00000490993.5:n.4156T>C (NPHP3)
ENST00000493732.5:n.131T>C (NPHP3)
ENST00000632629.1:c.78T>C (NPHP3-ACAD11)
NM_153240.4:c.3431T>C (NPHP3)	NP_694972.3:p.Leu1144Pro
NR_037804.1:n.3437T>C (NPHP3-ACAD11)
NM_153240.5:c.3431T>C (NPHP3) MANE Select	NP_694972.3:p.Leu1144Pro