Canonical Allele Identifier: CA338048829
Gene: NPHP4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.5863910A>G , CM000663.2:g.5863910A>G GRCh38
NC_000001.10:g.5923970A>G , CM000663.1:g.5923970A>G GRCh37
NC_000001.9:g.5846557A>G NCBI36
NG_011724.2:g.133562T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000378156.9:c.4120T>C MANE Select ENSP00000367398.4:p.Phe1374Leu
ENST00000378156.8:c.4120T>C ENSP00000367398.4:p.Phe1374Leu
ENST00000378161.5:n.3271T>C
ENST00000378169.7:c.*3021T>C ENSP00000367411.3:n.*3021T>C
ENST00000460696.1:n.2868T>C
ENST00000478423.6:n.3852T>C
ENST00000489180.6:c.*1931T>C ENSP00000423747.1:n.*1931T>C
NM_001291593.1:c.2581T>C NP_001278522.1:p.Phe861Leu
NM_001291594.1:c.2584T>C NP_001278523.1:p.Phe862Leu
NM_015102.4:c.4120T>C NP_055917.1:p.Phe1374Leu
NR_111987.1:n.4935T>C
XM_006710563.2:c.4120T>C XP_006710626.1:p.Phe1374Leu
XM_006710565.2:c.4120T>C XP_006710628.1:p.Phe1374Leu
XM_011541213.1:c.4117T>C XP_011539515.1:p.Phe1373Leu
XM_011541214.1:c.4078T>C XP_011539516.1:p.Phe1360Leu
XM_011541215.1:c.4009T>C XP_011539517.1:p.Phe1337Leu
XM_011541216.1:c.4120T>C XP_011539518.1:p.Phe1374Leu
XM_011541217.1:c.4120T>C XP_011539519.1:p.Phe1374Leu
XM_011541218.1:c.4120T>C XP_011539520.1:p.Phe1374Leu
XM_011541219.1:c.4066T>C XP_011539521.1:p.Phe1356Leu
XM_006710563.3:c.4120T>C XP_006710626.1:p.Phe1374Leu
XM_011541216.2:c.4120T>C XP_011539518.1:p.Phe1374Leu
XM_011541217.2:c.4120T>C XP_011539519.1:p.Phe1374Leu
XM_011541218.2:c.4120T>C XP_011539520.1:p.Phe1374Leu
XM_017000996.1:c.4075T>C XP_016856485.1:p.Phe1359Leu
XM_017000997.1:c.4120T>C XP_016856486.1:p.Phe1374Leu
XM_017000999.1:c.3592T>C XP_016856488.1:p.Phe1198Leu
XM_017001000.2:c.3592T>C XP_016856489.1:p.Phe1198Leu
XM_017001001.1:c.3322T>C XP_016856490.1:p.Phe1108Leu
XM_017001003.1:c.2581T>C XP_016856492.1:p.Phe861Leu
XR_001737114.1:n.3986T>C
XR_001737115.1:n.3971T>C
NM_015102.5:c.4120T>C MANE Select NP_055917.1:p.Phe1374Leu
NM_001291593.2:c.2581T>C NP_001278522.1:p.Phe861Leu
NM_001291594.2:c.2584T>C NP_001278523.1:p.Phe862Leu
NR_111987.2:n.4887T>C