Canonical Allele Identifier: CA2742301567

Gene: NPHP4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.5864126_5864145del , CM000663.2:g.5864126_5864145del	GRCh38
NC_000001.10:g.5924186_5924205del , CM000663.1:g.5924186_5924205del	GRCh37
NC_000001.9:g.5846773_5846792del	NCBI36
NG_011724.2:g.133327_133346del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378156.9:c.3997-112_3997-93del MANE Select	ENSP00000367398.4:n.3997-112_3997-93del
ENST00000378156.8:c.3997-112_3997-93del	ENSP00000367398.4:n.3997-112_3997-93del
ENST00000378161.5:n.3036_3055del
ENST00000378169.7:c.*2898-112_*2898-93del	ENSP00000367411.3:n.*2898-112_*2898-93del
ENST00000460696.1:n.2745-112_2745-93del
ENST00000478423.6:n.3729-112_3729-93del
ENST00000489180.6:c.*1808-112_*1808-93del	ENSP00000423747.1:n.*1808-112_*1808-93del
NM_001291593.1:c.2458-112_2458-93del	NP_001278522.1:n.2458-112_2458-93del
NM_001291594.1:c.2461-112_2461-93del	NP_001278523.1:n.2461-112_2461-93del
NM_015102.4:c.3997-112_3997-93del	NP_055917.1:n.3997-112_3997-93del
NR_111987.1:n.4812-112_4812-93del
XM_006710563.2:c.3997-112_3997-93del	XP_006710626.1:n.3997-112_3997-93del
XM_006710565.2:c.3997-112_3997-93del	XP_006710628.1:n.3997-112_3997-93del
XM_011541213.1:c.3994-112_3994-93del	XP_011539515.1:n.3994-112_3994-93del
XM_011541214.1:c.3955-112_3955-93del	XP_011539516.1:n.3955-112_3955-93del
XM_011541215.1:c.3886-112_3886-93del	XP_011539517.1:n.3886-112_3886-93del
XM_011541216.1:c.3997-112_3997-93del	XP_011539518.1:n.3997-112_3997-93del
XM_011541217.1:c.3997-112_3997-93del	XP_011539519.1:n.3997-112_3997-93del
XM_011541218.1:c.3997-112_3997-93del	XP_011539520.1:n.3997-112_3997-93del
XM_011541219.1:c.3943-112_3943-93del	XP_011539521.1:n.3943-112_3943-93del
XM_006710563.3:c.3997-112_3997-93del	XP_006710626.1:n.3997-112_3997-93del
XM_011541216.2:c.3997-112_3997-93del	XP_011539518.1:n.3997-112_3997-93del
XM_011541217.2:c.3997-112_3997-93del	XP_011539519.1:n.3997-112_3997-93del
XM_011541218.2:c.3997-112_3997-93del	XP_011539520.1:n.3997-112_3997-93del
XM_017000996.1:c.3952-112_3952-93del	XP_016856485.1:n.3952-112_3952-93del
XM_017000997.1:c.3997-112_3997-93del	XP_016856486.1:n.3997-112_3997-93del
XM_017000999.1:c.3469-112_3469-93del	XP_016856488.1:n.3469-112_3469-93del
XM_017001000.2:c.3469-112_3469-93del	XP_016856489.1:n.3469-112_3469-93del
XM_017001001.1:c.3199-112_3199-93del	XP_016856490.1:n.3199-112_3199-93del
XM_017001003.1:c.2458-112_2458-93del	XP_016856492.1:n.2458-112_2458-93del
XR_001737114.1:n.3863-112_3863-93del
XR_001737115.1:n.3848-112_3848-93del
NM_015102.5:c.3997-112_3997-93del MANE Select	NP_055917.1:n.3997-112_3997-93del
NM_001291593.2:c.2458-112_2458-93del	NP_001278522.1:n.2458-112_2458-93del
NM_001291594.2:c.2461-112_2461-93del	NP_001278523.1:n.2461-112_2461-93del
NR_111987.2:n.4764-112_4764-93del