Canonical Allele Identifier: CA1141549578

Gene: NPHP4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.5863137T= , CM000663.2:g.5863137T=	GRCh38
NC_000001.10:g.5923197T= , CM000663.1:g.5923197T=	GRCh37
NC_000001.9:g.5845784T=	NCBI36
NG_011724.2:g.134335A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000378156.9:c.*128A= MANE Select	ENSP00000367398.4:n.*128A=
ENST00000378156.8:c.*128A=	ENSP00000367398.4:n.*128A=
ENST00000378161.5:n.4044A=
ENST00000460696.1:n.3641A=
ENST00000478423.6:n.4141A=
ENST00000489180.6:c.*2220A=	ENSP00000423747.1:n.*2220A=
NM_001291593.1:c.*128A=	NP_001278522.1:n.*128A=
NM_001291594.1:c.*128A=	NP_001278523.1:n.*128A=
NM_015102.4:c.*128A=	NP_055917.1:n.*128A=
NR_111987.1:n.5224A=
XM_006710563.2:c.*128A=	XP_006710626.1:n.*128A=
XM_006710565.2:c.*128A=	XP_006710628.1:n.*128A=
XM_011541213.1:c.*128A=	XP_011539515.1:n.*128A=
XM_011541214.1:c.*128A=	XP_011539516.1:n.*128A=
XM_011541215.1:c.*128A=	XP_011539517.1:n.*128A=
XM_011541216.1:c.*128A=	XP_011539518.1:n.*128A=
XM_011541217.1:c.*128A=	XP_011539519.1:n.*128A=
XM_011541218.1:c.*128A=	XP_011539520.1:n.*128A=
XM_011541219.1:c.*128A=	XP_011539521.1:n.*128A=
XM_006710563.3:c.*128A=	XP_006710626.1:n.*128A=
XM_011541216.2:c.*128A=	XP_011539518.1:n.*128A=
XM_011541217.2:c.*128A=	XP_011539519.1:n.*128A=
XM_011541218.2:c.*128A=	XP_011539520.1:n.*128A=
XM_017000996.1:c.*128A=	XP_016856485.1:n.*128A=
XM_017000997.1:c.*128A=	XP_016856486.1:n.*128A=
XM_017000999.1:c.*128A=	XP_016856488.1:n.*128A=
XM_017001000.2:c.*128A=	XP_016856489.1:n.*128A=
XM_017001001.1:c.*128A=	XP_016856490.1:n.*128A=
XM_017001003.1:c.*128A=	XP_016856492.1:n.*128A=
XR_001737114.1:n.4275A=
XR_001737115.1:n.4260A=
NM_015102.5:c.*128A= MANE Select	NP_055917.1:n.*128A=
NM_001291593.2:c.*128A=	NP_001278522.1:n.*128A=
NM_001291594.2:c.*128A=	NP_001278523.1:n.*128A=
NR_111987.2:n.5176A=