Canonical Allele Identifier: CA354589172

Gene: NPHP3 NPHP3-ACAD11 NPHP3-AS1

Linked Data

• MyVariant Identifiers: chr3:g.132440935C>G (hg19) ; chr3:g.132722091C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.132722091C>G , CM000665.2:g.132722091C>G	GRCh38
NC_000003.11:g.132440935C>G , CM000665.1:g.132440935C>G	GRCh37
NC_000003.10:g.133923625C>G	NCBI36
NG_008130.1:g.5342G>C
NG_008130.2:g.5342G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683570.1:c.265G>C (NPHP3)	ENSP00000508409.1:p.Ala89Pro
ENST00000684294.1:c.99+166G>C (NPHP3)	ENSP00000508078.1:n.99+166G>C
ENST00000337331.10:c.265G>C (NPHP3) MANE Select	ENSP00000338766.5:p.Ala89Pro
ENST00000337331.9:c.265G>C (NPHP3)	ENSP00000338766.5:p.Ala89Pro
ENST00000383282.3:c.265G>C (NPHP3-ACAD11)	ENSP00000372769.2:p.Ala89Pro
ENST00000465756.5:c.99+166G>C (NPHP3)	ENSP00000419907.1:n.99+166G>C
ENST00000471702.2:c.265G>C (NPHP3-ACAD11)	ENSP00000419763.1:p.Ala89Pro
NM_153240.4:c.265G>C (NPHP3)	NP_694972.3:p.Ala89Pro
NR_037804.1:n.369G>C (NPHP3-ACAD11)
NR_002811.2:n.342C>G (NPHP3-AS1)
NR_152743.1:n.342C>G (NPHP3-AS1)
NM_153240.5:c.265G>C (NPHP3) MANE Select	NP_694972.3:p.Ala89Pro