Canonical Allele Identifier: CA1151209496

Gene: NPHP4

Linked Data

• dbSNP Id: rs1640942210
• gnomAD v4: 1-5864180-GGA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.5864185_5864186del , CM000663.2:g.5864185_5864186del	GRCh38
NC_000001.10:g.5924245_5924246del , CM000663.1:g.5924245_5924246del	GRCh37
NC_000001.9:g.5846832_5846833del	NCBI36
NG_011724.2:g.133290_133291del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378156.9:c.3997-149_3997-148del MANE Select	ENSP00000367398.4:n.3997-149_3997-148del
ENST00000378156.8:c.3997-149_3997-148del	ENSP00000367398.4:n.3997-149_3997-148del
ENST00000378161.5:n.2999_3000del
ENST00000378169.7:c.*2898-149_*2898-148del	ENSP00000367411.3:n.*2898-149_*2898-148del
ENST00000460696.1:n.2745-149_2745-148del
ENST00000478423.6:n.3729-149_3729-148del
ENST00000489180.6:c.*1808-149_*1808-148del	ENSP00000423747.1:n.*1808-149_*1808-148del
NM_001291593.1:c.2458-149_2458-148del	NP_001278522.1:n.2458-149_2458-148del
NM_001291594.1:c.2461-149_2461-148del	NP_001278523.1:n.2461-149_2461-148del
NM_015102.4:c.3997-149_3997-148del	NP_055917.1:n.3997-149_3997-148del
NR_111987.1:n.4812-149_4812-148del
XM_006710563.2:c.3997-149_3997-148del	XP_006710626.1:n.3997-149_3997-148del
XM_006710565.2:c.3997-149_3997-148del	XP_006710628.1:n.3997-149_3997-148del
XM_011541213.1:c.3994-149_3994-148del	XP_011539515.1:n.3994-149_3994-148del
XM_011541214.1:c.3955-149_3955-148del	XP_011539516.1:n.3955-149_3955-148del
XM_011541215.1:c.3886-149_3886-148del	XP_011539517.1:n.3886-149_3886-148del
XM_011541216.1:c.3997-149_3997-148del	XP_011539518.1:n.3997-149_3997-148del
XM_011541217.1:c.3997-149_3997-148del	XP_011539519.1:n.3997-149_3997-148del
XM_011541218.1:c.3997-149_3997-148del	XP_011539520.1:n.3997-149_3997-148del
XM_011541219.1:c.3943-149_3943-148del	XP_011539521.1:n.3943-149_3943-148del
XM_006710563.3:c.3997-149_3997-148del	XP_006710626.1:n.3997-149_3997-148del
XM_011541216.2:c.3997-149_3997-148del	XP_011539518.1:n.3997-149_3997-148del
XM_011541217.2:c.3997-149_3997-148del	XP_011539519.1:n.3997-149_3997-148del
XM_011541218.2:c.3997-149_3997-148del	XP_011539520.1:n.3997-149_3997-148del
XM_017000996.1:c.3952-149_3952-148del	XP_016856485.1:n.3952-149_3952-148del
XM_017000997.1:c.3997-149_3997-148del	XP_016856486.1:n.3997-149_3997-148del
XM_017000999.1:c.3469-149_3469-148del	XP_016856488.1:n.3469-149_3469-148del
XM_017001000.2:c.3469-149_3469-148del	XP_016856489.1:n.3469-149_3469-148del
XM_017001001.1:c.3199-149_3199-148del	XP_016856490.1:n.3199-149_3199-148del
XM_017001003.1:c.2458-149_2458-148del	XP_016856492.1:n.2458-149_2458-148del
XR_001737114.1:n.3863-149_3863-148del
XR_001737115.1:n.3848-149_3848-148del
NM_015102.5:c.3997-149_3997-148del MANE Select	NP_055917.1:n.3997-149_3997-148del
NM_001291593.2:c.2458-149_2458-148del	NP_001278522.1:n.2458-149_2458-148del
NM_001291594.2:c.2461-149_2461-148del	NP_001278523.1:n.2461-149_2461-148del
NR_111987.2:n.4764-149_4764-148del