Canonical Allele Identifier: CA415787048
Gene: NPHP4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.5924082G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.5864022G>T , CM000663.2:g.5864022G>T GRCh38
NC_000001.10:g.5924082G>T , CM000663.1:g.5924082G>T GRCh37
NC_000001.9:g.5846669G>T NCBI36
NG_011724.2:g.133450C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000378156.9:c.4008C>A MANE Select ENSP00000367398.4:p.Ile1336=
ENST00000378156.8:c.4008C>A ENSP00000367398.4:p.Ile1336=
ENST00000378161.5:n.3159C>A
ENST00000378169.7:c.*2909C>A ENSP00000367411.3:n.*2909C>A
ENST00000460696.1:n.2756C>A
ENST00000478423.6:n.3740C>A
ENST00000489180.6:c.*1819C>A ENSP00000423747.1:n.*1819C>A
NM_001291593.1:c.2469C>A NP_001278522.1:p.Ile823=
NM_001291594.1:c.2472C>A NP_001278523.1:p.Ile824=
NM_015102.4:c.4008C>A NP_055917.1:p.Ile1336=
NR_111987.1:n.4823C>A
XM_006710563.2:c.4008C>A XP_006710626.1:p.Ile1336=
XM_006710565.2:c.4008C>A XP_006710628.1:p.Ile1336=
XM_011541213.1:c.4005C>A XP_011539515.1:p.Ile1335=
XM_011541214.1:c.3966C>A XP_011539516.1:p.Ile1322=
XM_011541215.1:c.3897C>A XP_011539517.1:p.Ile1299=
XM_011541216.1:c.4008C>A XP_011539518.1:p.Ile1336=
XM_011541217.1:c.4008C>A XP_011539519.1:p.Ile1336=
XM_011541218.1:c.4008C>A XP_011539520.1:p.Ile1336=
XM_011541219.1:c.3954C>A XP_011539521.1:p.Ile1318=
XM_006710563.3:c.4008C>A XP_006710626.1:p.Ile1336=
XM_011541216.2:c.4008C>A XP_011539518.1:p.Ile1336=
XM_011541217.2:c.4008C>A XP_011539519.1:p.Ile1336=
XM_011541218.2:c.4008C>A XP_011539520.1:p.Ile1336=
XM_017000996.1:c.3963C>A XP_016856485.1:p.Ile1321=
XM_017000997.1:c.4008C>A XP_016856486.1:p.Ile1336=
XM_017000999.1:c.3480C>A XP_016856488.1:p.Ile1160=
XM_017001000.2:c.3480C>A XP_016856489.1:p.Ile1160=
XM_017001001.1:c.3210C>A XP_016856490.1:p.Ile1070=
XM_017001003.1:c.2469C>A XP_016856492.1:p.Ile823=
XR_001737114.1:n.3874C>A
XR_001737115.1:n.3859C>A
NM_015102.5:c.4008C>A MANE Select NP_055917.1:p.Ile1336=
NM_001291593.2:c.2469C>A NP_001278522.1:p.Ile823=
NM_001291594.2:c.2472C>A NP_001278523.1:p.Ile824=
NR_111987.2:n.4775C>A