Canonical Allele Identifier: CA2742301517

Gene: NPHP4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.5864070_5864071insA , CM000663.2:g.5864070_5864071insA	GRCh38
NC_000001.10:g.5924130_5924131insA , CM000663.1:g.5924130_5924131insA	GRCh37
NC_000001.9:g.5846717_5846718insA	NCBI36
NG_011724.2:g.133401_133402insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378156.9:c.3997-38_3997-37insT MANE Select	ENSP00000367398.4:n.3997-38_3997-37insT
ENST00000378156.8:c.3997-38_3997-37insT	ENSP00000367398.4:n.3997-38_3997-37insT
ENST00000378161.5:n.3110_3111insT
ENST00000378169.7:c.*2898-38_*2898-37insT	ENSP00000367411.3:n.*2898-38_*2898-37insT
ENST00000460696.1:n.2745-38_2745-37insT
ENST00000478423.6:n.3729-38_3729-37insT
ENST00000489180.6:c.*1808-38_*1808-37insT	ENSP00000423747.1:n.*1808-38_*1808-37insT
NM_001291593.1:c.2458-38_2458-37insT	NP_001278522.1:n.2458-38_2458-37insT
NM_001291594.1:c.2461-38_2461-37insT	NP_001278523.1:n.2461-38_2461-37insT
NM_015102.4:c.3997-38_3997-37insT	NP_055917.1:n.3997-38_3997-37insT
NR_111987.1:n.4812-38_4812-37insT
XM_006710563.2:c.3997-38_3997-37insT	XP_006710626.1:n.3997-38_3997-37insT
XM_006710565.2:c.3997-38_3997-37insT	XP_006710628.1:n.3997-38_3997-37insT
XM_011541213.1:c.3994-38_3994-37insT	XP_011539515.1:n.3994-38_3994-37insT
XM_011541214.1:c.3955-38_3955-37insT	XP_011539516.1:n.3955-38_3955-37insT
XM_011541215.1:c.3886-38_3886-37insT	XP_011539517.1:n.3886-38_3886-37insT
XM_011541216.1:c.3997-38_3997-37insT	XP_011539518.1:n.3997-38_3997-37insT
XM_011541217.1:c.3997-38_3997-37insT	XP_011539519.1:n.3997-38_3997-37insT
XM_011541218.1:c.3997-38_3997-37insT	XP_011539520.1:n.3997-38_3997-37insT
XM_011541219.1:c.3943-38_3943-37insT	XP_011539521.1:n.3943-38_3943-37insT
XM_006710563.3:c.3997-38_3997-37insT	XP_006710626.1:n.3997-38_3997-37insT
XM_011541216.2:c.3997-38_3997-37insT	XP_011539518.1:n.3997-38_3997-37insT
XM_011541217.2:c.3997-38_3997-37insT	XP_011539519.1:n.3997-38_3997-37insT
XM_011541218.2:c.3997-38_3997-37insT	XP_011539520.1:n.3997-38_3997-37insT
XM_017000996.1:c.3952-38_3952-37insT	XP_016856485.1:n.3952-38_3952-37insT
XM_017000997.1:c.3997-38_3997-37insT	XP_016856486.1:n.3997-38_3997-37insT
XM_017000999.1:c.3469-38_3469-37insT	XP_016856488.1:n.3469-38_3469-37insT
XM_017001000.2:c.3469-38_3469-37insT	XP_016856489.1:n.3469-38_3469-37insT
XM_017001001.1:c.3199-38_3199-37insT	XP_016856490.1:n.3199-38_3199-37insT
XM_017001003.1:c.2458-38_2458-37insT	XP_016856492.1:n.2458-38_2458-37insT
XR_001737114.1:n.3863-38_3863-37insT
XR_001737115.1:n.3848-38_3848-37insT
NM_015102.5:c.3997-38_3997-37insT MANE Select	NP_055917.1:n.3997-38_3997-37insT
NM_001291593.2:c.2458-38_2458-37insT	NP_001278522.1:n.2458-38_2458-37insT
NM_001291594.2:c.2461-38_2461-37insT	NP_001278523.1:n.2461-38_2461-37insT
NR_111987.2:n.4764-38_4764-37insT