Canonical Allele Identifier: CA415786952

Gene: NPHP4

Linked Data

• dbSNP Id: rs2100370971
• MyVariant Identifiers: chr1:g.5923965T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.5863905T>C , CM000663.2:g.5863905T>C	GRCh38
NC_000001.10:g.5923965T>C , CM000663.1:g.5923965T>C	GRCh37
NC_000001.9:g.5846552T>C	NCBI36
NG_011724.2:g.133567A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378156.9:c.4125A>G MANE Select	ENSP00000367398.4:p.Arg1375=
ENST00000378156.8:c.4125A>G	ENSP00000367398.4:p.Arg1375=
ENST00000378161.5:n.3276A>G
ENST00000378169.7:c.*3026A>G	ENSP00000367411.3:n.*3026A>G
ENST00000460696.1:n.2873A>G
ENST00000478423.6:n.3857A>G
ENST00000489180.6:c.*1936A>G	ENSP00000423747.1:n.*1936A>G
NM_001291593.1:c.2586A>G	NP_001278522.1:p.Arg862=
NM_001291594.1:c.2589A>G	NP_001278523.1:p.Arg863=
NM_015102.4:c.4125A>G	NP_055917.1:p.Arg1375=
NR_111987.1:n.4940A>G
XM_006710563.2:c.4125A>G	XP_006710626.1:p.Arg1375=
XM_006710565.2:c.4125A>G	XP_006710628.1:p.Arg1375=
XM_011541213.1:c.4122A>G	XP_011539515.1:p.Arg1374=
XM_011541214.1:c.4083A>G	XP_011539516.1:p.Arg1361=
XM_011541215.1:c.4014A>G	XP_011539517.1:p.Arg1338=
XM_011541216.1:c.4125A>G	XP_011539518.1:p.Arg1375=
XM_011541217.1:c.4125A>G	XP_011539519.1:p.Arg1375=
XM_011541218.1:c.4125A>G	XP_011539520.1:p.Arg1375=
XM_011541219.1:c.4071A>G	XP_011539521.1:p.Arg1357=
XM_006710563.3:c.4125A>G	XP_006710626.1:p.Arg1375=
XM_011541216.2:c.4125A>G	XP_011539518.1:p.Arg1375=
XM_011541217.2:c.4125A>G	XP_011539519.1:p.Arg1375=
XM_011541218.2:c.4125A>G	XP_011539520.1:p.Arg1375=
XM_017000996.1:c.4080A>G	XP_016856485.1:p.Arg1360=
XM_017000997.1:c.4125A>G	XP_016856486.1:p.Arg1375=
XM_017000999.1:c.3597A>G	XP_016856488.1:p.Arg1199=
XM_017001000.2:c.3597A>G	XP_016856489.1:p.Arg1199=
XM_017001001.1:c.3327A>G	XP_016856490.1:p.Arg1109=
XM_017001003.1:c.2586A>G	XP_016856492.1:p.Arg862=
XR_001737114.1:n.3991A>G
XR_001737115.1:n.3976A>G
NM_015102.5:c.4125A>G MANE Select	NP_055917.1:p.Arg1375=
NM_001291593.2:c.2586A>G	NP_001278522.1:p.Arg862=
NM_001291594.2:c.2589A>G	NP_001278523.1:p.Arg863=
NR_111987.2:n.4892A>G