Canonical Allele Identifier: CA354580310
Gene: NPHP3 HGNC NCBI
NPHP3-ACAD11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.132689097T>G , CM000665.2:g.132689097T>G GRCh38
NC_000003.11:g.132407941T>G , CM000665.1:g.132407941T>G GRCh37
NC_000003.10:g.133890631T>G NCBI36
NG_008130.1:g.38336A>C
NG_008130.2:g.38336A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000684294.1:c.*768A>C (NPHP3) ENSP00000508078.1:n.*768A>C
ENST00000337331.10:c.2860A>C (NPHP3) MANE Select ENSP00000338766.5:p.Lys954Gln
ENST00000337331.9:c.2860A>C (NPHP3) ENSP00000338766.5:p.Lys954Gln
ENST00000465756.5:c.*768A>C (NPHP3) ENSP00000419907.1:n.*768A>C
ENST00000471702.2:c.*851A>C (NPHP3-ACAD11) ENSP00000419763.1:n.*851A>C
ENST00000474871.5:n.594A>C (NPHP3)
ENST00000490993.5:n.3585A>C (NPHP3)
NM_153240.4:c.2860A>C (NPHP3) NP_694972.3:p.Lys954Gln
NR_037804.1:n.2866A>C (NPHP3-ACAD11)
NM_153240.5:c.2860A>C (NPHP3) MANE Select NP_694972.3:p.Lys954Gln