Canonical Allele Identifier: CA338048799
Gene: NPHP4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.5863903T>G , CM000663.2:g.5863903T>G GRCh38
NC_000001.10:g.5923963T>G , CM000663.1:g.5923963T>G GRCh37
NC_000001.9:g.5846550T>G NCBI36
NG_011724.2:g.133569A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000378156.9:c.4127A>C MANE Select ENSP00000367398.4:p.Glu1376Ala
ENST00000378156.8:c.4127A>C ENSP00000367398.4:p.Glu1376Ala
ENST00000378161.5:n.3278A>C
ENST00000378169.7:c.*3028A>C ENSP00000367411.3:n.*3028A>C
ENST00000460696.1:n.2875A>C
ENST00000478423.6:n.3859A>C
ENST00000489180.6:c.*1938A>C ENSP00000423747.1:n.*1938A>C
NM_001291593.1:c.2588A>C NP_001278522.1:p.Glu863Ala
NM_001291594.1:c.2591A>C NP_001278523.1:p.Glu864Ala
NM_015102.4:c.4127A>C NP_055917.1:p.Glu1376Ala
NR_111987.1:n.4942A>C
XM_006710563.2:c.4127A>C XP_006710626.1:p.Glu1376Ala
XM_006710565.2:c.4127A>C XP_006710628.1:p.Glu1376Ala
XM_011541213.1:c.4124A>C XP_011539515.1:p.Glu1375Ala
XM_011541214.1:c.4085A>C XP_011539516.1:p.Glu1362Ala
XM_011541215.1:c.4016A>C XP_011539517.1:p.Glu1339Ala
XM_011541216.1:c.4127A>C XP_011539518.1:p.Glu1376Ala
XM_011541217.1:c.4127A>C XP_011539519.1:p.Glu1376Ala
XM_011541218.1:c.4127A>C XP_011539520.1:p.Glu1376Ala
XM_011541219.1:c.4073A>C XP_011539521.1:p.Glu1358Ala
XM_006710563.3:c.4127A>C XP_006710626.1:p.Glu1376Ala
XM_011541216.2:c.4127A>C XP_011539518.1:p.Glu1376Ala
XM_011541217.2:c.4127A>C XP_011539519.1:p.Glu1376Ala
XM_011541218.2:c.4127A>C XP_011539520.1:p.Glu1376Ala
XM_017000996.1:c.4082A>C XP_016856485.1:p.Glu1361Ala
XM_017000997.1:c.4127A>C XP_016856486.1:p.Glu1376Ala
XM_017000999.1:c.3599A>C XP_016856488.1:p.Glu1200Ala
XM_017001000.2:c.3599A>C XP_016856489.1:p.Glu1200Ala
XM_017001001.1:c.3329A>C XP_016856490.1:p.Glu1110Ala
XM_017001003.1:c.2588A>C XP_016856492.1:p.Glu863Ala
XR_001737114.1:n.3993A>C
XR_001737115.1:n.3978A>C
NM_015102.5:c.4127A>C MANE Select NP_055917.1:p.Glu1376Ala
NM_001291593.2:c.2588A>C NP_001278522.1:p.Glu863Ala
NM_001291594.2:c.2591A>C NP_001278523.1:p.Glu864Ala
NR_111987.2:n.4894A>C