Canonical Allele Identifier: CA435780796

Gene: NPHP3 NPHP3-ACAD11

Linked Data

• MyVariant Identifiers: chr3:g.132400838A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.132681994A>T , CM000665.2:g.132681994A>T	GRCh38
NC_000003.11:g.132400838A>T , CM000665.1:g.132400838A>T	GRCh37
NC_000003.10:g.133883528A>T	NCBI36
NG_008130.1:g.45439T>A
NG_008130.2:g.45439T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000684294.1:c.*1837T>A (NPHP3)	ENSP00000508078.1:n.*1837T>A
ENST00000337331.10:c.3909T>A (NPHP3) MANE Select	ENSP00000338766.5:p.Pro1303=
ENST00000337331.9:c.3909T>A (NPHP3)	ENSP00000338766.5:p.Pro1303=
ENST00000465756.5:c.*1817T>A (NPHP3)	ENSP00000419907.1:n.*1817T>A
ENST00000471702.2:c.*1900T>A (NPHP3-ACAD11)	ENSP00000419763.1:n.*1900T>A
ENST00000474871.5:n.3108T>A (NPHP3)
ENST00000490993.5:n.4634T>A (NPHP3)
ENST00000493732.5:n.1221T>A (NPHP3)
ENST00000512094.5:c.355T>A (NPHP3)	ENSP00000427666.1:n.355T>A
ENST00000632629.1:c.556T>A (NPHP3-ACAD11)
NM_153240.4:c.3909T>A (NPHP3)	NP_694972.3:p.Pro1303=
NR_037804.1:n.3915T>A (NPHP3-ACAD11)
NM_153240.5:c.3909T>A (NPHP3) MANE Select	NP_694972.3:p.Pro1303=