Canonical Allele Identifier: CA1151209090

Gene: NPHP4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.5863908G= , CM000663.2:g.5863908G=	GRCh38
NC_000001.10:g.5923968G= , CM000663.1:g.5923968G=	GRCh37
NC_000001.9:g.5846555G=	NCBI36
NG_011724.2:g.133564C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378156.9:c.4122C= MANE Select	ENSP00000367398.4:p.Phe1374=
ENST00000378156.8:c.4122C=	ENSP00000367398.4:p.Phe1374=
ENST00000378161.5:n.3273C=
ENST00000378169.7:c.*3023C=	ENSP00000367411.3:n.*3023C=
ENST00000460696.1:n.2870C=
ENST00000478423.6:n.3854C=
ENST00000489180.6:c.*1933C=	ENSP00000423747.1:n.*1933C=
NM_001291593.1:c.2583C=	NP_001278522.1:p.Phe861=
NM_001291594.1:c.2586C=	NP_001278523.1:p.Phe862=
NM_015102.4:c.4122C=	NP_055917.1:p.Phe1374=
NR_111987.1:n.4937C=
XM_006710563.2:c.4122C=	XP_006710626.1:p.Phe1374=
XM_006710565.2:c.4122C=	XP_006710628.1:p.Phe1374=
XM_011541213.1:c.4119C=	XP_011539515.1:p.Phe1373=
XM_011541214.1:c.4080C=	XP_011539516.1:p.Phe1360=
XM_011541215.1:c.4011C=	XP_011539517.1:p.Phe1337=
XM_011541216.1:c.4122C=	XP_011539518.1:p.Phe1374=
XM_011541217.1:c.4122C=	XP_011539519.1:p.Phe1374=
XM_011541218.1:c.4122C=	XP_011539520.1:p.Phe1374=
XM_011541219.1:c.4068C=	XP_011539521.1:p.Phe1356=
XM_006710563.3:c.4122C=	XP_006710626.1:p.Phe1374=
XM_011541216.2:c.4122C=	XP_011539518.1:p.Phe1374=
XM_011541217.2:c.4122C=	XP_011539519.1:p.Phe1374=
XM_011541218.2:c.4122C=	XP_011539520.1:p.Phe1374=
XM_017000996.1:c.4077C=	XP_016856485.1:p.Phe1359=
XM_017000997.1:c.4122C=	XP_016856486.1:p.Phe1374=
XM_017000999.1:c.3594C=	XP_016856488.1:p.Phe1198=
XM_017001000.2:c.3594C=	XP_016856489.1:p.Phe1198=
XM_017001001.1:c.3324C=	XP_016856490.1:p.Phe1108=
XM_017001003.1:c.2583C=	XP_016856492.1:p.Phe861=
XR_001737114.1:n.3988C=
XR_001737115.1:n.3973C=
NM_015102.5:c.4122C= MANE Select	NP_055917.1:p.Phe1374=
NM_001291593.2:c.2583C=	NP_001278522.1:p.Phe861=
NM_001291594.2:c.2586C=	NP_001278523.1:p.Phe862=
NR_111987.2:n.4889C=