Canonical Allele Identifier: CA1151208322

Gene: NPHP4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.5863160C= , CM000663.2:g.5863160C=	GRCh38
NC_000001.10:g.5923220C= , CM000663.1:g.5923220C=	GRCh37
NC_000001.9:g.5845807C=	NCBI36
NG_011724.2:g.134312G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000378156.9:c.*105G= MANE Select	ENSP00000367398.4:n.*105G=
ENST00000378156.8:c.*105G=	ENSP00000367398.4:n.*105G=
ENST00000378161.5:n.4021G=
ENST00000460696.1:n.3618G=
ENST00000478423.6:n.4118G=
ENST00000489180.6:c.*2197G=	ENSP00000423747.1:n.*2197G=
NM_001291593.1:c.*105G=	NP_001278522.1:n.*105G=
NM_001291594.1:c.*105G=	NP_001278523.1:n.*105G=
NM_015102.4:c.*105G=	NP_055917.1:n.*105G=
NR_111987.1:n.5201G=
XM_006710563.2:c.*105G=	XP_006710626.1:n.*105G=
XM_006710565.2:c.*105G=	XP_006710628.1:n.*105G=
XM_011541213.1:c.*105G=	XP_011539515.1:n.*105G=
XM_011541214.1:c.*105G=	XP_011539516.1:n.*105G=
XM_011541215.1:c.*105G=	XP_011539517.1:n.*105G=
XM_011541216.1:c.*105G=	XP_011539518.1:n.*105G=
XM_011541217.1:c.*105G=	XP_011539519.1:n.*105G=
XM_011541218.1:c.*105G=	XP_011539520.1:n.*105G=
XM_011541219.1:c.*105G=	XP_011539521.1:n.*105G=
XM_006710563.3:c.*105G=	XP_006710626.1:n.*105G=
XM_011541216.2:c.*105G=	XP_011539518.1:n.*105G=
XM_011541217.2:c.*105G=	XP_011539519.1:n.*105G=
XM_011541218.2:c.*105G=	XP_011539520.1:n.*105G=
XM_017000996.1:c.*105G=	XP_016856485.1:n.*105G=
XM_017000997.1:c.*105G=	XP_016856486.1:n.*105G=
XM_017000999.1:c.*105G=	XP_016856488.1:n.*105G=
XM_017001000.2:c.*105G=	XP_016856489.1:n.*105G=
XM_017001001.1:c.*105G=	XP_016856490.1:n.*105G=
XM_017001003.1:c.*105G=	XP_016856492.1:n.*105G=
XR_001737114.1:n.4252G=
XR_001737115.1:n.4237G=
NM_015102.5:c.*105G= MANE Select	NP_055917.1:n.*105G=
NM_001291593.2:c.*105G=	NP_001278522.1:n.*105G=
NM_001291594.2:c.*105G=	NP_001278523.1:n.*105G=
NR_111987.2:n.5153G=