Canonical Allele Identifier: CA83610545

Gene: NPHP3 NPHP3-ACAD11 NPHP3-AS1

Linked Data

• dbSNP Id: rs769597647
• gnomAD v4: 3-132721936-C-T
• MyVariant Identifiers: chr3:g.132440780C>T (hg19) ; chr3:g.132721936C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.132721936C>T , CM000665.2:g.132721936C>T	GRCh38
NC_000003.11:g.132440780C>T , CM000665.1:g.132440780C>T	GRCh37
NC_000003.10:g.133923470C>T	NCBI36
NG_008130.1:g.5497G>A
NG_008130.2:g.5497G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683570.1:c.420G>A (NPHP3)	ENSP00000508409.1:p.Pro140=
ENST00000684294.1:c.99+321G>A (NPHP3)	ENSP00000508078.1:n.99+321G>A
ENST00000684756.1:n.116+27G>A (NPHP3)
ENST00000337331.10:c.393+27G>A (NPHP3) MANE Select	ENSP00000338766.5:n.393+27G>A
ENST00000337331.9:c.393+27G>A (NPHP3)	ENSP00000338766.5:n.393+27G>A
ENST00000383282.3:c.393+27G>A (NPHP3-ACAD11)	ENSP00000372769.2:n.393+27G>A
ENST00000465756.5:c.99+321G>A (NPHP3)	ENSP00000419907.1:n.99+321G>A
ENST00000469232.5:c.45+27G>A (NPHP3)	ENSP00000418664.1:n.45+27G>A
ENST00000471702.2:c.393+27G>A (NPHP3-ACAD11)	ENSP00000419763.1:n.393+27G>A
NM_153240.4:c.393+27G>A (NPHP3)	NP_694972.3:n.393+27G>A
NR_037804.1:n.497+27G>A (NPHP3-ACAD11)
NR_002811.2:n.187C>T (NPHP3-AS1)
NR_152743.1:n.187C>T (NPHP3-AS1)
NM_153240.5:c.393+27G>A (NPHP3) MANE Select	NP_694972.3:n.393+27G>A