Canonical Allele Identifier: CA338049194
Gene: NPHP4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.5864004T>G , CM000663.2:g.5864004T>G GRCh38
NC_000001.10:g.5924064T>G , CM000663.1:g.5924064T>G GRCh37
NC_000001.9:g.5846651T>G NCBI36
NG_011724.2:g.133468A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000378156.9:c.4026A>C MANE Select ENSP00000367398.4:p.Glu1342Asp
ENST00000378156.8:c.4026A>C ENSP00000367398.4:p.Glu1342Asp
ENST00000378161.5:n.3177A>C
ENST00000378169.7:c.*2927A>C ENSP00000367411.3:n.*2927A>C
ENST00000460696.1:n.2774A>C
ENST00000478423.6:n.3758A>C
ENST00000489180.6:c.*1837A>C ENSP00000423747.1:n.*1837A>C
NM_001291593.1:c.2487A>C NP_001278522.1:p.Glu829Asp
NM_001291594.1:c.2490A>C NP_001278523.1:p.Glu830Asp
NM_015102.4:c.4026A>C NP_055917.1:p.Glu1342Asp
NR_111987.1:n.4841A>C
XM_006710563.2:c.4026A>C XP_006710626.1:p.Glu1342Asp
XM_006710565.2:c.4026A>C XP_006710628.1:p.Glu1342Asp
XM_011541213.1:c.4023A>C XP_011539515.1:p.Glu1341Asp
XM_011541214.1:c.3984A>C XP_011539516.1:p.Glu1328Asp
XM_011541215.1:c.3915A>C XP_011539517.1:p.Glu1305Asp
XM_011541216.1:c.4026A>C XP_011539518.1:p.Glu1342Asp
XM_011541217.1:c.4026A>C XP_011539519.1:p.Glu1342Asp
XM_011541218.1:c.4026A>C XP_011539520.1:p.Glu1342Asp
XM_011541219.1:c.3972A>C XP_011539521.1:p.Glu1324Asp
XM_006710563.3:c.4026A>C XP_006710626.1:p.Glu1342Asp
XM_011541216.2:c.4026A>C XP_011539518.1:p.Glu1342Asp
XM_011541217.2:c.4026A>C XP_011539519.1:p.Glu1342Asp
XM_011541218.2:c.4026A>C XP_011539520.1:p.Glu1342Asp
XM_017000996.1:c.3981A>C XP_016856485.1:p.Glu1327Asp
XM_017000997.1:c.4026A>C XP_016856486.1:p.Glu1342Asp
XM_017000999.1:c.3498A>C XP_016856488.1:p.Glu1166Asp
XM_017001000.2:c.3498A>C XP_016856489.1:p.Glu1166Asp
XM_017001001.1:c.3228A>C XP_016856490.1:p.Glu1076Asp
XM_017001003.1:c.2487A>C XP_016856492.1:p.Glu829Asp
XR_001737114.1:n.3892A>C
XR_001737115.1:n.3877A>C
NM_015102.5:c.4026A>C MANE Select NP_055917.1:p.Glu1342Asp
NM_001291593.2:c.2487A>C NP_001278522.1:p.Glu829Asp
NM_001291594.2:c.2490A>C NP_001278523.1:p.Glu830Asp
NR_111987.2:n.4793A>C