Canonical Allele Identifier: CA1402637866
Gene: NPHP3 HGNC NCBI
NPHP3-ACAD11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.132700426A= , CM000665.2:g.132700426A= GRCh38
NC_000003.11:g.132419270A= , CM000665.1:g.132419270A= GRCh37
NC_000003.10:g.133901960A= NCBI36
NG_008130.1:g.27007T=
NG_008130.2:g.27007T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000684294.1:c.1357T= (NPHP3) ENSP00000508078.1:p.Ser453=
ENST00000337331.10:c.1651T= (NPHP3) MANE Select ENSP00000338766.5:p.Ser551=
ENST00000337331.9:c.1651T= (NPHP3) ENSP00000338766.5:p.Ser551=
ENST00000465756.5:c.1357T= (NPHP3) ENSP00000419907.1:p.Ser453=
ENST00000469232.5:c.1466T= (NPHP3) ENSP00000418664.1:n.1466T=
ENST00000471702.2:c.1651T= (NPHP3-ACAD11) ENSP00000419763.1:p.Ser551=
ENST00000490993.5:n.1427T= (NPHP3)
NM_153240.4:c.1651T= (NPHP3) NP_694972.3:p.Ser551=
NR_037804.1:n.1755T= (NPHP3-ACAD11)
NM_153240.5:c.1651T= (NPHP3) MANE Select NP_694972.3:p.Ser551=