Canonical Allele Identifier: CA2742301593

Gene: NPHP4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.5864161_5864162insA , CM000663.2:g.5864161_5864162insA	GRCh38
NC_000001.10:g.5924221_5924222insA , CM000663.1:g.5924221_5924222insA	GRCh37
NC_000001.9:g.5846808_5846809insA	NCBI36
NG_011724.2:g.133310_133311insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378156.9:c.3997-129_3997-128insT MANE Select	ENSP00000367398.4:n.3997-129_3997-128insT
ENST00000378156.8:c.3997-129_3997-128insT	ENSP00000367398.4:n.3997-129_3997-128insT
ENST00000378161.5:n.3019_3020insT
ENST00000378169.7:c.*2898-129_*2898-128insT	ENSP00000367411.3:n.*2898-129_*2898-128insT
ENST00000460696.1:n.2745-129_2745-128insT
ENST00000478423.6:n.3729-129_3729-128insT
ENST00000489180.6:c.*1808-129_*1808-128insT	ENSP00000423747.1:n.*1808-129_*1808-128insT
NM_001291593.1:c.2458-129_2458-128insT	NP_001278522.1:n.2458-129_2458-128insT
NM_001291594.1:c.2461-129_2461-128insT	NP_001278523.1:n.2461-129_2461-128insT
NM_015102.4:c.3997-129_3997-128insT	NP_055917.1:n.3997-129_3997-128insT
NR_111987.1:n.4812-129_4812-128insT
XM_006710563.2:c.3997-129_3997-128insT	XP_006710626.1:n.3997-129_3997-128insT
XM_006710565.2:c.3997-129_3997-128insT	XP_006710628.1:n.3997-129_3997-128insT
XM_011541213.1:c.3994-129_3994-128insT	XP_011539515.1:n.3994-129_3994-128insT
XM_011541214.1:c.3955-129_3955-128insT	XP_011539516.1:n.3955-129_3955-128insT
XM_011541215.1:c.3886-129_3886-128insT	XP_011539517.1:n.3886-129_3886-128insT
XM_011541216.1:c.3997-129_3997-128insT	XP_011539518.1:n.3997-129_3997-128insT
XM_011541217.1:c.3997-129_3997-128insT	XP_011539519.1:n.3997-129_3997-128insT
XM_011541218.1:c.3997-129_3997-128insT	XP_011539520.1:n.3997-129_3997-128insT
XM_011541219.1:c.3943-129_3943-128insT	XP_011539521.1:n.3943-129_3943-128insT
XM_006710563.3:c.3997-129_3997-128insT	XP_006710626.1:n.3997-129_3997-128insT
XM_011541216.2:c.3997-129_3997-128insT	XP_011539518.1:n.3997-129_3997-128insT
XM_011541217.2:c.3997-129_3997-128insT	XP_011539519.1:n.3997-129_3997-128insT
XM_011541218.2:c.3997-129_3997-128insT	XP_011539520.1:n.3997-129_3997-128insT
XM_017000996.1:c.3952-129_3952-128insT	XP_016856485.1:n.3952-129_3952-128insT
XM_017000997.1:c.3997-129_3997-128insT	XP_016856486.1:n.3997-129_3997-128insT
XM_017000999.1:c.3469-129_3469-128insT	XP_016856488.1:n.3469-129_3469-128insT
XM_017001000.2:c.3469-129_3469-128insT	XP_016856489.1:n.3469-129_3469-128insT
XM_017001001.1:c.3199-129_3199-128insT	XP_016856490.1:n.3199-129_3199-128insT
XM_017001003.1:c.2458-129_2458-128insT	XP_016856492.1:n.2458-129_2458-128insT
XR_001737114.1:n.3863-129_3863-128insT
XR_001737115.1:n.3848-129_3848-128insT
NM_015102.5:c.3997-129_3997-128insT MANE Select	NP_055917.1:n.3997-129_3997-128insT
NM_001291593.2:c.2458-129_2458-128insT	NP_001278522.1:n.2458-129_2458-128insT
NM_001291594.2:c.2461-129_2461-128insT	NP_001278523.1:n.2461-129_2461-128insT
NR_111987.2:n.4764-129_4764-128insT