Canonical Allele Identifier: CA1151209272

Gene: NPHP4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.5864006C= , CM000663.2:g.5864006C=	GRCh38
NC_000001.10:g.5924066C= , CM000663.1:g.5924066C=	GRCh37
NC_000001.9:g.5846653C=	NCBI36
NG_011724.2:g.133466G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378156.9:c.4024G= MANE Select	ENSP00000367398.4:p.Glu1342=
ENST00000378156.8:c.4024G=	ENSP00000367398.4:p.Glu1342=
ENST00000378161.5:n.3175G=
ENST00000378169.7:c.*2925G=	ENSP00000367411.3:n.*2925G=
ENST00000460696.1:n.2772G=
ENST00000478423.6:n.3756G=
ENST00000489180.6:c.*1835G=	ENSP00000423747.1:n.*1835G=
NM_001291593.1:c.2485G=	NP_001278522.1:p.Glu829=
NM_001291594.1:c.2488G=	NP_001278523.1:p.Glu830=
NM_015102.4:c.4024G=	NP_055917.1:p.Glu1342=
NR_111987.1:n.4839G=
XM_006710563.2:c.4024G=	XP_006710626.1:p.Glu1342=
XM_006710565.2:c.4024G=	XP_006710628.1:p.Glu1342=
XM_011541213.1:c.4021G=	XP_011539515.1:p.Glu1341=
XM_011541214.1:c.3982G=	XP_011539516.1:p.Glu1328=
XM_011541215.1:c.3913G=	XP_011539517.1:p.Glu1305=
XM_011541216.1:c.4024G=	XP_011539518.1:p.Glu1342=
XM_011541217.1:c.4024G=	XP_011539519.1:p.Glu1342=
XM_011541218.1:c.4024G=	XP_011539520.1:p.Glu1342=
XM_011541219.1:c.3970G=	XP_011539521.1:p.Glu1324=
XM_006710563.3:c.4024G=	XP_006710626.1:p.Glu1342=
XM_011541216.2:c.4024G=	XP_011539518.1:p.Glu1342=
XM_011541217.2:c.4024G=	XP_011539519.1:p.Glu1342=
XM_011541218.2:c.4024G=	XP_011539520.1:p.Glu1342=
XM_017000996.1:c.3979G=	XP_016856485.1:p.Glu1327=
XM_017000997.1:c.4024G=	XP_016856486.1:p.Glu1342=
XM_017000999.1:c.3496G=	XP_016856488.1:p.Glu1166=
XM_017001000.2:c.3496G=	XP_016856489.1:p.Glu1166=
XM_017001001.1:c.3226G=	XP_016856490.1:p.Glu1076=
XM_017001003.1:c.2485G=	XP_016856492.1:p.Glu829=
XR_001737114.1:n.3890G=
XR_001737115.1:n.3875G=
NM_015102.5:c.4024G= MANE Select	NP_055917.1:p.Glu1342=
NM_001291593.2:c.2485G=	NP_001278522.1:p.Glu829=
NM_001291594.2:c.2488G=	NP_001278523.1:p.Glu830=
NR_111987.2:n.4791G=