Canonical Allele Identifier: CA436088319
Gene: NPHP3 HGNC NCBI
NPHP3-ACAD11 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.132407927A>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.132689083A>T , CM000665.2:g.132689083A>T GRCh38
NC_000003.11:g.132407927A>T , CM000665.1:g.132407927A>T GRCh37
NC_000003.10:g.133890617A>T NCBI36
NG_008130.1:g.38350T>A
NG_008130.2:g.38350T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000684294.1:c.*782T>A (NPHP3) ENSP00000508078.1:n.*782T>A
ENST00000337331.10:c.2874T>A (NPHP3) MANE Select ENSP00000338766.5:p.Leu958=
ENST00000337331.9:c.2874T>A (NPHP3) ENSP00000338766.5:p.Leu958=
ENST00000465756.5:c.*782T>A (NPHP3) ENSP00000419907.1:n.*782T>A
ENST00000471702.2:c.*865T>A (NPHP3-ACAD11) ENSP00000419763.1:n.*865T>A
ENST00000474871.5:n.608T>A (NPHP3)
ENST00000490993.5:n.3599T>A (NPHP3)
NM_153240.4:c.2874T>A (NPHP3) NP_694972.3:p.Leu958=
NR_037804.1:n.2880T>A (NPHP3-ACAD11)
NM_153240.5:c.2874T>A (NPHP3) MANE Select NP_694972.3:p.Leu958=
Search 100 bp 5'
Search 100 bp 3'