Canonical Allele Identifier: CA338047260
Gene: NPHP4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.5863288A>C , CM000663.2:g.5863288A>C GRCh38
NC_000001.10:g.5923348A>C , CM000663.1:g.5923348A>C GRCh37
NC_000001.9:g.5845935A>C NCBI36
NG_011724.2:g.134184T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000378156.9:c.4258T>G MANE Select ENSP00000367398.4:p.Cys1420Gly
ENST00000378156.8:c.4258T>G ENSP00000367398.4:p.Cys1420Gly
ENST00000378161.5:n.3893T>G
ENST00000378169.7:c.*3159T>G ENSP00000367411.3:n.*3159T>G
ENST00000460696.1:n.3490T>G
ENST00000478423.6:n.3990T>G
ENST00000489180.6:c.*2069T>G ENSP00000423747.1:n.*2069T>G
NM_001291593.1:c.2719T>G NP_001278522.1:p.Cys907Gly
NM_001291594.1:c.2722T>G NP_001278523.1:p.Cys908Gly
NM_015102.4:c.4258T>G NP_055917.1:p.Cys1420Gly
NR_111987.1:n.5073T>G
XM_006710563.2:c.4258T>G XP_006710626.1:p.Cys1420Gly
XM_006710565.2:c.4258T>G XP_006710628.1:p.Cys1420Gly
XM_011541213.1:c.4255T>G XP_011539515.1:p.Cys1419Gly
XM_011541214.1:c.4216T>G XP_011539516.1:p.Cys1406Gly
XM_011541215.1:c.4147T>G XP_011539517.1:p.Cys1383Gly
XM_011541216.1:c.4258T>G XP_011539518.1:p.Cys1420Gly
XM_011541217.1:c.4258T>G XP_011539519.1:p.Cys1420Gly
XM_011541218.1:c.4258T>G XP_011539520.1:p.Cys1420Gly
XM_011541219.1:c.4204T>G XP_011539521.1:p.Cys1402Gly
XM_006710563.3:c.4258T>G XP_006710626.1:p.Cys1420Gly
XM_011541216.2:c.4258T>G XP_011539518.1:p.Cys1420Gly
XM_011541217.2:c.4258T>G XP_011539519.1:p.Cys1420Gly
XM_011541218.2:c.4258T>G XP_011539520.1:p.Cys1420Gly
XM_017000996.1:c.4213T>G XP_016856485.1:p.Cys1405Gly
XM_017000997.1:c.4258T>G XP_016856486.1:p.Cys1420Gly
XM_017000999.1:c.3730T>G XP_016856488.1:p.Cys1244Gly
XM_017001000.2:c.3730T>G XP_016856489.1:p.Cys1244Gly
XM_017001001.1:c.3460T>G XP_016856490.1:p.Cys1154Gly
XM_017001003.1:c.2719T>G XP_016856492.1:p.Cys907Gly
XR_001737114.1:n.4124T>G
XR_001737115.1:n.4109T>G
NM_015102.5:c.4258T>G MANE Select NP_055917.1:p.Cys1420Gly
NM_001291593.2:c.2719T>G NP_001278522.1:p.Cys907Gly
NM_001291594.2:c.2722T>G NP_001278523.1:p.Cys908Gly
NR_111987.2:n.5025T>G