Canonical Allele Identifier: CA436088462

Gene: NPHP3 NPHP3-ACAD11

Linked Data

• MyVariant Identifiers: chr3:g.132407975T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.132689131T>C , CM000665.2:g.132689131T>C	GRCh38
NC_000003.11:g.132407975T>C , CM000665.1:g.132407975T>C	GRCh37
NC_000003.10:g.133890665T>C	NCBI36
NG_008130.1:g.38302A>G
NG_008130.2:g.38302A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684294.1:c.*734A>G (NPHP3)	ENSP00000508078.1:n.*734A>G
ENST00000337331.10:c.2826A>G (NPHP3) MANE Select	ENSP00000338766.5:p.Leu942=
ENST00000337331.9:c.2826A>G (NPHP3)	ENSP00000338766.5:p.Leu942=
ENST00000465756.5:c.*734A>G (NPHP3)	ENSP00000419907.1:n.*734A>G
ENST00000471702.2:c.*817A>G (NPHP3-ACAD11)	ENSP00000419763.1:n.*817A>G
ENST00000474871.5:n.560A>G (NPHP3)
ENST00000490993.5:n.3551A>G (NPHP3)
NM_153240.4:c.2826A>G (NPHP3)	NP_694972.3:p.Leu942=
NR_037804.1:n.2832A>G (NPHP3-ACAD11)
NM_153240.5:c.2826A>G (NPHP3) MANE Select	NP_694972.3:p.Leu942=