Canonical Allele Identifier: CA354580630
Gene: NPHP3 HGNC NCBI
NPHP3-ACAD11 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.132408079A>G (hg19) chr3:g.132689235A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.132689235A>G , CM000665.2:g.132689235A>G GRCh38
NC_000003.11:g.132408079A>G , CM000665.1:g.132408079A>G GRCh37
NC_000003.10:g.133890769A>G NCBI36
NG_008130.1:g.38198T>C
NG_008130.2:g.38198T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000684294.1:c.*630T>C (NPHP3) ENSP00000508078.1:n.*630T>C
ENST00000337331.10:c.2722T>C (NPHP3) MANE Select ENSP00000338766.5:p.Trp908Arg
ENST00000337331.9:c.2722T>C (NPHP3) ENSP00000338766.5:p.Trp908Arg
ENST00000465756.5:c.*630T>C (NPHP3) ENSP00000419907.1:n.*630T>C
ENST00000471702.2:c.*713T>C (NPHP3-ACAD11) ENSP00000419763.1:n.*713T>C
ENST00000474871.5:n.456T>C (NPHP3)
ENST00000490993.5:n.3447T>C (NPHP3)
NM_153240.4:c.2722T>C (NPHP3) NP_694972.3:p.Trp908Arg
NR_037804.1:n.2728T>C (NPHP3-ACAD11)
NM_153240.5:c.2722T>C (NPHP3) MANE Select NP_694972.3:p.Trp908Arg
Search 100 bp 5'
Search 100 bp 3'