Canonical Allele Identifier: CA415787054
Gene: NPHP4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.5924091G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.5864031G>T , CM000663.2:g.5864031G>T GRCh38
NC_000001.10:g.5924091G>T , CM000663.1:g.5924091G>T GRCh37
NC_000001.9:g.5846678G>T NCBI36
NG_011724.2:g.133441C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000378156.9:c.3999C>A MANE Select ENSP00000367398.4:p.Ala1333=
ENST00000378156.8:c.3999C>A ENSP00000367398.4:p.Ala1333=
ENST00000378161.5:n.3150C>A
ENST00000378169.7:c.*2900C>A ENSP00000367411.3:n.*2900C>A
ENST00000460696.1:n.2747C>A
ENST00000478423.6:n.3731C>A
ENST00000489180.6:c.*1810C>A ENSP00000423747.1:n.*1810C>A
NM_001291593.1:c.2460C>A NP_001278522.1:p.Ala820=
NM_001291594.1:c.2463C>A NP_001278523.1:p.Ala821=
NM_015102.4:c.3999C>A NP_055917.1:p.Ala1333=
NR_111987.1:n.4814C>A
XM_006710563.2:c.3999C>A XP_006710626.1:p.Ala1333=
XM_006710565.2:c.3999C>A XP_006710628.1:p.Ala1333=
XM_011541213.1:c.3996C>A XP_011539515.1:p.Ala1332=
XM_011541214.1:c.3957C>A XP_011539516.1:p.Ala1319=
XM_011541215.1:c.3888C>A XP_011539517.1:p.Ala1296=
XM_011541216.1:c.3999C>A XP_011539518.1:p.Ala1333=
XM_011541217.1:c.3999C>A XP_011539519.1:p.Ala1333=
XM_011541218.1:c.3999C>A XP_011539520.1:p.Ala1333=
XM_011541219.1:c.3945C>A XP_011539521.1:p.Ala1315=
XM_006710563.3:c.3999C>A XP_006710626.1:p.Ala1333=
XM_011541216.2:c.3999C>A XP_011539518.1:p.Ala1333=
XM_011541217.2:c.3999C>A XP_011539519.1:p.Ala1333=
XM_011541218.2:c.3999C>A XP_011539520.1:p.Ala1333=
XM_017000996.1:c.3954C>A XP_016856485.1:p.Ala1318=
XM_017000997.1:c.3999C>A XP_016856486.1:p.Ala1333=
XM_017000999.1:c.3471C>A XP_016856488.1:p.Ala1157=
XM_017001000.2:c.3471C>A XP_016856489.1:p.Ala1157=
XM_017001001.1:c.3201C>A XP_016856490.1:p.Ala1067=
XM_017001003.1:c.2460C>A XP_016856492.1:p.Ala820=
XR_001737114.1:n.3865C>A
XR_001737115.1:n.3850C>A
NM_015102.5:c.3999C>A MANE Select NP_055917.1:p.Ala1333=
NM_001291593.2:c.2460C>A NP_001278522.1:p.Ala820=
NM_001291594.2:c.2463C>A NP_001278523.1:p.Ala821=
NR_111987.2:n.4766C>A