Canonical Allele Identifier: CA338048780
Gene: NPHP4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.5863899G>T , CM000663.2:g.5863899G>T GRCh38
NC_000001.10:g.5923959G>T , CM000663.1:g.5923959G>T GRCh37
NC_000001.9:g.5846546G>T NCBI36
NG_011724.2:g.133573C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000378156.9:c.4131C>A MANE Select ENSP00000367398.4:p.Asp1377Glu
ENST00000378156.8:c.4131C>A ENSP00000367398.4:p.Asp1377Glu
ENST00000378161.5:n.3282C>A
ENST00000378169.7:c.*3032C>A ENSP00000367411.3:n.*3032C>A
ENST00000460696.1:n.2879C>A
ENST00000478423.6:n.3863C>A
ENST00000489180.6:c.*1942C>A ENSP00000423747.1:n.*1942C>A
NM_001291593.1:c.2592C>A NP_001278522.1:p.Asp864Glu
NM_001291594.1:c.2595C>A NP_001278523.1:p.Asp865Glu
NM_015102.4:c.4131C>A NP_055917.1:p.Asp1377Glu
NR_111987.1:n.4946C>A
XM_006710563.2:c.4131C>A XP_006710626.1:p.Asp1377Glu
XM_006710565.2:c.4131C>A XP_006710628.1:p.Asp1377Glu
XM_011541213.1:c.4128C>A XP_011539515.1:p.Asp1376Glu
XM_011541214.1:c.4089C>A XP_011539516.1:p.Asp1363Glu
XM_011541215.1:c.4020C>A XP_011539517.1:p.Asp1340Glu
XM_011541216.1:c.4131C>A XP_011539518.1:p.Asp1377Glu
XM_011541217.1:c.4131C>A XP_011539519.1:p.Asp1377Glu
XM_011541218.1:c.4131C>A XP_011539520.1:p.Asp1377Glu
XM_011541219.1:c.4077C>A XP_011539521.1:p.Asp1359Glu
XM_006710563.3:c.4131C>A XP_006710626.1:p.Asp1377Glu
XM_011541216.2:c.4131C>A XP_011539518.1:p.Asp1377Glu
XM_011541217.2:c.4131C>A XP_011539519.1:p.Asp1377Glu
XM_011541218.2:c.4131C>A XP_011539520.1:p.Asp1377Glu
XM_017000996.1:c.4086C>A XP_016856485.1:p.Asp1362Glu
XM_017000997.1:c.4131C>A XP_016856486.1:p.Asp1377Glu
XM_017000999.1:c.3603C>A XP_016856488.1:p.Asp1201Glu
XM_017001000.2:c.3603C>A XP_016856489.1:p.Asp1201Glu
XM_017001001.1:c.3333C>A XP_016856490.1:p.Asp1111Glu
XM_017001003.1:c.2592C>A XP_016856492.1:p.Asp864Glu
XR_001737114.1:n.3997C>A
XR_001737115.1:n.3982C>A
NM_015102.5:c.4131C>A MANE Select NP_055917.1:p.Asp1377Glu
NM_001291593.2:c.2592C>A NP_001278522.1:p.Asp864Glu
NM_001291594.2:c.2595C>A NP_001278523.1:p.Asp865Glu
NR_111987.2:n.4898C>A