Canonical Allele Identifier: CA2577904956
Gene: NPHP3 HGNC NCBI
NPHP3-ACAD11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.132684893dup , CM000665.2:g.132684893dup GRCh38
NC_000003.11:g.132403737dup , CM000665.1:g.132403737dup GRCh37
NC_000003.10:g.133886427dup NCBI36
NG_008130.1:g.42540dup
NG_008130.2:g.42540dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000684294.1:c.*1238-99dup (NPHP3) ENSP00000508078.1:n.*1238-99dup
ENST00000337331.10:c.3330-99dup (NPHP3) MANE Select ENSP00000338766.5:n.3330-99dup
ENST00000337331.9:c.3330-99dup (NPHP3) ENSP00000338766.5:n.3330-99dup
ENST00000465756.5:c.*1238-99dup (NPHP3) ENSP00000419907.1:n.*1238-99dup
ENST00000471702.2:c.*1321-99dup (NPHP3-ACAD11) ENSP00000419763.1:n.*1321-99dup
ENST00000474871.5:n.2430dup (NPHP3)
ENST00000490993.5:n.4055-99dup (NPHP3)
NM_153240.4:c.3330-99dup (NPHP3) NP_694972.3:n.3330-99dup
NR_037804.1:n.3336-99dup (NPHP3-ACAD11)
NM_153240.5:c.3330-99dup (NPHP3) MANE Select NP_694972.3:n.3330-99dup