Canonical Allele Identifier: CA2667736473

Gene: NPHP3 NPHP3-ACAD11

Linked Data

• gnomAD v4: 3-132684885-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.132684885T>G , CM000665.2:g.132684885T>G	GRCh38
NC_000003.11:g.132403729T>G , CM000665.1:g.132403729T>G	GRCh37
NC_000003.10:g.133886419T>G	NCBI36
NG_008130.1:g.42548A>C
NG_008130.2:g.42548A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684294.1:c.*1238-91A>C (NPHP3)	ENSP00000508078.1:n.*1238-91A>C
ENST00000337331.10:c.3330-91A>C (NPHP3) MANE Select	ENSP00000338766.5:n.3330-91A>C
ENST00000337331.9:c.3330-91A>C (NPHP3)	ENSP00000338766.5:n.3330-91A>C
ENST00000465756.5:c.*1238-91A>C (NPHP3)	ENSP00000419907.1:n.*1238-91A>C
ENST00000471702.2:c.*1321-91A>C (NPHP3-ACAD11)	ENSP00000419763.1:n.*1321-91A>C
ENST00000474871.5:n.2438A>C (NPHP3)
ENST00000490993.5:n.4055-91A>C (NPHP3)
NM_153240.4:c.3330-91A>C (NPHP3)	NP_694972.3:n.3330-91A>C
NR_037804.1:n.3336-91A>C (NPHP3-ACAD11)
NM_153240.5:c.3330-91A>C (NPHP3) MANE Select	NP_694972.3:n.3330-91A>C