Canonical Allele Identifier: CA338048789
Gene: NPHP4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.5863901C>T , CM000663.2:g.5863901C>T GRCh38
NC_000001.10:g.5923961C>T , CM000663.1:g.5923961C>T GRCh37
NC_000001.9:g.5846548C>T NCBI36
NG_011724.2:g.133571G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000378156.9:c.4129G>A MANE Select ENSP00000367398.4:p.Asp1377Asn
ENST00000378156.8:c.4129G>A ENSP00000367398.4:p.Asp1377Asn
ENST00000378161.5:n.3280G>A
ENST00000378169.7:c.*3030G>A ENSP00000367411.3:n.*3030G>A
ENST00000460696.1:n.2877G>A
ENST00000478423.6:n.3861G>A
ENST00000489180.6:c.*1940G>A ENSP00000423747.1:n.*1940G>A
NM_001291593.1:c.2590G>A NP_001278522.1:p.Asp864Asn
NM_001291594.1:c.2593G>A NP_001278523.1:p.Asp865Asn
NM_015102.4:c.4129G>A NP_055917.1:p.Asp1377Asn
NR_111987.1:n.4944G>A
XM_006710563.2:c.4129G>A XP_006710626.1:p.Asp1377Asn
XM_006710565.2:c.4129G>A XP_006710628.1:p.Asp1377Asn
XM_011541213.1:c.4126G>A XP_011539515.1:p.Asp1376Asn
XM_011541214.1:c.4087G>A XP_011539516.1:p.Asp1363Asn
XM_011541215.1:c.4018G>A XP_011539517.1:p.Asp1340Asn
XM_011541216.1:c.4129G>A XP_011539518.1:p.Asp1377Asn
XM_011541217.1:c.4129G>A XP_011539519.1:p.Asp1377Asn
XM_011541218.1:c.4129G>A XP_011539520.1:p.Asp1377Asn
XM_011541219.1:c.4075G>A XP_011539521.1:p.Asp1359Asn
XM_006710563.3:c.4129G>A XP_006710626.1:p.Asp1377Asn
XM_011541216.2:c.4129G>A XP_011539518.1:p.Asp1377Asn
XM_011541217.2:c.4129G>A XP_011539519.1:p.Asp1377Asn
XM_011541218.2:c.4129G>A XP_011539520.1:p.Asp1377Asn
XM_017000996.1:c.4084G>A XP_016856485.1:p.Asp1362Asn
XM_017000997.1:c.4129G>A XP_016856486.1:p.Asp1377Asn
XM_017000999.1:c.3601G>A XP_016856488.1:p.Asp1201Asn
XM_017001000.2:c.3601G>A XP_016856489.1:p.Asp1201Asn
XM_017001001.1:c.3331G>A XP_016856490.1:p.Asp1111Asn
XM_017001003.1:c.2590G>A XP_016856492.1:p.Asp864Asn
XR_001737114.1:n.3995G>A
XR_001737115.1:n.3980G>A
NM_015102.5:c.4129G>A MANE Select NP_055917.1:p.Asp1377Asn
NM_001291593.2:c.2590G>A NP_001278522.1:p.Asp864Asn
NM_001291594.2:c.2593G>A NP_001278523.1:p.Asp865Asn
NR_111987.2:n.4896G>A