Canonical Allele Identifier: CA554537
Community Standard Title: NM_015102.5(NPHP4):c.1376C>A (p.Thr459Lys)
Gene: NPHP4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.5927714G>T , CM000663.2:g.5927714G>T GRCh38
NC_000001.10:g.5987774G>T , CM000663.1:g.5987774G>T GRCh37
NC_000001.9:g.5910361G>T NCBI36
NG_011724.2:g.69758C>A

Transcript Alleles

HGVS Amino-acid Change
NM_015102.5:c.1376C>A MANE Select NP_055917.1:p.Thr459Lys
ENST00000378156.9:c.1376C>A MANE Select ENSP00000367398.4:p.Thr459Lys
NM_001291593.1:c.10C>A NP_001278522.1:p.Arg4=
NM_001291593.2:c.10C>A NP_001278522.1:p.Arg4=
NM_001291594.1:c.10C>A NP_001278523.1:p.Arg4=
NM_001291594.2:c.10C>A NP_001278523.1:p.Arg4=
NM_015102.4:c.1376C>A NP_055917.1:p.Thr459Lys
NR_111987.1:n.1644C>A
NR_111987.2:n.1596C>A
ENST00000378156.8:c.1376C>A ENSP00000367398.4:p.Thr459Lys
ENST00000378169.7:c.*450C>A ENSP00000367411.3:n.*450C>A
ENST00000478423.6:n.1278C>A
ENST00000489180.6:c.1376C>A ENSP00000423747.1:p.Thr459Lys
ENST00000622020.4:c.1376C>A ENSP00000481831.2:p.Thr459Lys
XM_006710563.2:c.1376C>A XP_006710626.1:p.Thr459Lys
XM_006710563.3:c.1376C>A XP_006710626.1:p.Thr459Lys
XM_006710565.2:c.1376C>A XP_006710628.1:p.Thr459Lys
XM_011541213.1:c.1376C>A XP_011539515.1:p.Thr459Lys
XM_011541214.1:c.1376C>A XP_011539516.1:p.Thr459Lys
XM_011541215.1:c.1376C>A XP_011539517.1:p.Thr459Lys
XM_011541216.1:c.1376C>A XP_011539518.1:p.Thr459Lys
XM_011541216.2:c.1376C>A XP_011539518.1:p.Thr459Lys
XM_011541217.1:c.1376C>A XP_011539519.1:p.Thr459Lys
XM_011541217.2:c.1376C>A XP_011539519.1:p.Thr459Lys
XM_011541218.1:c.1376C>A XP_011539520.1:p.Thr459Lys
XM_011541218.2:c.1376C>A XP_011539520.1:p.Thr459Lys
XM_011541219.1:c.1322C>A XP_011539521.1:p.Thr441Lys
XM_011541220.1:c.1376C>A XP_011539522.1:p.Thr459Lys
XM_017000996.1:c.1376C>A XP_016856485.1:p.Thr459Lys
XM_017000997.1:c.1376C>A XP_016856486.1:p.Thr459Lys
XM_017000998.1:c.1376C>A XP_016856487.1:p.Thr459Lys
XM_017000999.1:c.848C>A XP_016856488.1:p.Thr283Lys
XM_017001000.2:c.848C>A XP_016856489.1:p.Thr283Lys
XM_017001001.1:c.578C>A XP_016856490.1:p.Thr193Lys
XM_017001002.1:c.1376C>A XP_016856491.1:p.Thr459Lys
XM_017001003.1:c.10C>A XP_016856492.1:p.Arg4=
XR_001737114.1:n.1414C>A
XR_001737115.1:n.1414C>A
XR_946604.1:n.1414C>A
XR_946605.1:n.1414C>A