Canonical Allele Identifier: CA2642901954

Gene: NPHP4

Linked Data

• gnomAD v4: 1-5864118-TGTGCACC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.5864125_5864131del , CM000663.2:g.5864125_5864131del	GRCh38
NC_000001.10:g.5924185_5924191del , CM000663.1:g.5924185_5924191del	GRCh37
NC_000001.9:g.5846772_5846778del	NCBI36
NG_011724.2:g.133347_133353del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378156.9:c.3997-92_3997-86del MANE Select	ENSP00000367398.4:n.3997-92_3997-86del
ENST00000378156.8:c.3997-92_3997-86del	ENSP00000367398.4:n.3997-92_3997-86del
ENST00000378161.5:n.3056_3062del
ENST00000378169.7:c.*2898-92_*2898-86del	ENSP00000367411.3:n.*2898-92_*2898-86del
ENST00000460696.1:n.2745-92_2745-86del
ENST00000478423.6:n.3729-92_3729-86del
ENST00000489180.6:c.*1808-92_*1808-86del	ENSP00000423747.1:n.*1808-92_*1808-86del
NM_001291593.1:c.2458-92_2458-86del	NP_001278522.1:n.2458-92_2458-86del
NM_001291594.1:c.2461-92_2461-86del	NP_001278523.1:n.2461-92_2461-86del
NM_015102.4:c.3997-92_3997-86del	NP_055917.1:n.3997-92_3997-86del
NR_111987.1:n.4812-92_4812-86del
XM_006710563.2:c.3997-92_3997-86del	XP_006710626.1:n.3997-92_3997-86del
XM_006710565.2:c.3997-92_3997-86del	XP_006710628.1:n.3997-92_3997-86del
XM_011541213.1:c.3994-92_3994-86del	XP_011539515.1:n.3994-92_3994-86del
XM_011541214.1:c.3955-92_3955-86del	XP_011539516.1:n.3955-92_3955-86del
XM_011541215.1:c.3886-92_3886-86del	XP_011539517.1:n.3886-92_3886-86del
XM_011541216.1:c.3997-92_3997-86del	XP_011539518.1:n.3997-92_3997-86del
XM_011541217.1:c.3997-92_3997-86del	XP_011539519.1:n.3997-92_3997-86del
XM_011541218.1:c.3997-92_3997-86del	XP_011539520.1:n.3997-92_3997-86del
XM_011541219.1:c.3943-92_3943-86del	XP_011539521.1:n.3943-92_3943-86del
XM_006710563.3:c.3997-92_3997-86del	XP_006710626.1:n.3997-92_3997-86del
XM_011541216.2:c.3997-92_3997-86del	XP_011539518.1:n.3997-92_3997-86del
XM_011541217.2:c.3997-92_3997-86del	XP_011539519.1:n.3997-92_3997-86del
XM_011541218.2:c.3997-92_3997-86del	XP_011539520.1:n.3997-92_3997-86del
XM_017000996.1:c.3952-92_3952-86del	XP_016856485.1:n.3952-92_3952-86del
XM_017000997.1:c.3997-92_3997-86del	XP_016856486.1:n.3997-92_3997-86del
XM_017000999.1:c.3469-92_3469-86del	XP_016856488.1:n.3469-92_3469-86del
XM_017001000.2:c.3469-92_3469-86del	XP_016856489.1:n.3469-92_3469-86del
XM_017001001.1:c.3199-92_3199-86del	XP_016856490.1:n.3199-92_3199-86del
XM_017001003.1:c.2458-92_2458-86del	XP_016856492.1:n.2458-92_2458-86del
XR_001737114.1:n.3863-92_3863-86del
XR_001737115.1:n.3848-92_3848-86del
NM_015102.5:c.3997-92_3997-86del MANE Select	NP_055917.1:n.3997-92_3997-86del
NM_001291593.2:c.2458-92_2458-86del	NP_001278522.1:n.2458-92_2458-86del
NM_001291594.2:c.2461-92_2461-86del	NP_001278523.1:n.2461-92_2461-86del
NR_111987.2:n.4764-92_4764-86del