Canonical Allele Identifier: CA436088732

Gene: NPHP3 NPHP3-ACAD11

Linked Data

• gnomAD v4: 3-132689254-A-G
• MyVariant Identifiers: chr3:g.132408098A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.132689254A>G , CM000665.2:g.132689254A>G	GRCh38
NC_000003.11:g.132408098A>G , CM000665.1:g.132408098A>G	GRCh37
NC_000003.10:g.133890788A>G	NCBI36
NG_008130.1:g.38179T>C
NG_008130.2:g.38179T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684294.1:c.*611T>C (NPHP3)	ENSP00000508078.1:n.*611T>C
ENST00000337331.10:c.2703T>C (NPHP3) MANE Select	ENSP00000338766.5:p.Phe901=
ENST00000337331.9:c.2703T>C (NPHP3)	ENSP00000338766.5:p.Phe901=
ENST00000465756.5:c.*611T>C (NPHP3)	ENSP00000419907.1:n.*611T>C
ENST00000471702.2:c.*694T>C (NPHP3-ACAD11)	ENSP00000419763.1:n.*694T>C
ENST00000474871.5:n.437T>C (NPHP3)
ENST00000490993.5:n.3428T>C (NPHP3)
NM_153240.4:c.2703T>C (NPHP3)	NP_694972.3:p.Phe901=
NR_037804.1:n.2709T>C (NPHP3-ACAD11)
NM_153240.5:c.2703T>C (NPHP3) MANE Select	NP_694972.3:p.Phe901=