Canonical Allele Identifier: CA415786953

Gene: NPHP4

Linked Data

• MyVariant Identifiers: chr1:g.5923967T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.5863907T>G , CM000663.2:g.5863907T>G	GRCh38
NC_000001.10:g.5923967T>G , CM000663.1:g.5923967T>G	GRCh37
NC_000001.9:g.5846554T>G	NCBI36
NG_011724.2:g.133565A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378156.9:c.4123A>C MANE Select	ENSP00000367398.4:p.Arg1375=
ENST00000378156.8:c.4123A>C	ENSP00000367398.4:p.Arg1375=
ENST00000378161.5:n.3274A>C
ENST00000378169.7:c.*3024A>C	ENSP00000367411.3:n.*3024A>C
ENST00000460696.1:n.2871A>C
ENST00000478423.6:n.3855A>C
ENST00000489180.6:c.*1934A>C	ENSP00000423747.1:n.*1934A>C
NM_001291593.1:c.2584A>C	NP_001278522.1:p.Arg862=
NM_001291594.1:c.2587A>C	NP_001278523.1:p.Arg863=
NM_015102.4:c.4123A>C	NP_055917.1:p.Arg1375=
NR_111987.1:n.4938A>C
XM_006710563.2:c.4123A>C	XP_006710626.1:p.Arg1375=
XM_006710565.2:c.4123A>C	XP_006710628.1:p.Arg1375=
XM_011541213.1:c.4120A>C	XP_011539515.1:p.Arg1374=
XM_011541214.1:c.4081A>C	XP_011539516.1:p.Arg1361=
XM_011541215.1:c.4012A>C	XP_011539517.1:p.Arg1338=
XM_011541216.1:c.4123A>C	XP_011539518.1:p.Arg1375=
XM_011541217.1:c.4123A>C	XP_011539519.1:p.Arg1375=
XM_011541218.1:c.4123A>C	XP_011539520.1:p.Arg1375=
XM_011541219.1:c.4069A>C	XP_011539521.1:p.Arg1357=
XM_006710563.3:c.4123A>C	XP_006710626.1:p.Arg1375=
XM_011541216.2:c.4123A>C	XP_011539518.1:p.Arg1375=
XM_011541217.2:c.4123A>C	XP_011539519.1:p.Arg1375=
XM_011541218.2:c.4123A>C	XP_011539520.1:p.Arg1375=
XM_017000996.1:c.4078A>C	XP_016856485.1:p.Arg1360=
XM_017000997.1:c.4123A>C	XP_016856486.1:p.Arg1375=
XM_017000999.1:c.3595A>C	XP_016856488.1:p.Arg1199=
XM_017001000.2:c.3595A>C	XP_016856489.1:p.Arg1199=
XM_017001001.1:c.3325A>C	XP_016856490.1:p.Arg1109=
XM_017001003.1:c.2584A>C	XP_016856492.1:p.Arg862=
XR_001737114.1:n.3989A>C
XR_001737115.1:n.3974A>C
NM_015102.5:c.4123A>C MANE Select	NP_055917.1:p.Arg1375=
NM_001291593.2:c.2584A>C	NP_001278522.1:p.Arg862=
NM_001291594.2:c.2587A>C	NP_001278523.1:p.Arg863=
NR_111987.2:n.4890A>C