Canonical Allele Identifier: CA338058773

Gene: NPHP4

Linked Data

• MyVariant Identifiers: chr1:g.5947474A>T (hg19) ; chr1:g.5887414A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.5887414A>T , CM000663.2:g.5887414A>T	GRCh38
NC_000001.10:g.5947474A>T , CM000663.1:g.5947474A>T	GRCh37
NC_000001.9:g.5870061A>T	NCBI36
NG_011724.2:g.110058T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000378156.9:c.2357T>A MANE Select	ENSP00000367398.4:p.Val786Asp
ENST00000378156.8:c.2357T>A	ENSP00000367398.4:p.Val786Asp
ENST00000378169.7:c.*1258T>A	ENSP00000367411.3:n.*1258T>A
ENST00000466897.1:c.586T>A
ENST00000478423.6:n.2089T>A
ENST00000489180.6:c.2354T>A	ENSP00000423747.1:p.Val785Asp
ENST00000622020.4:c.2354T>A	ENSP00000481831.2:p.Val785Asp
NM_001291593.1:c.818T>A	NP_001278522.1:p.Val273Asp
NM_001291594.1:c.821T>A	NP_001278523.1:p.Val274Asp
NM_015102.4:c.2357T>A	NP_055917.1:p.Val786Asp
NR_111987.1:n.2622T>A
XM_006710563.2:c.2357T>A	XP_006710626.1:p.Val786Asp
XM_006710565.2:c.2357T>A	XP_006710628.1:p.Val786Asp
XM_011541213.1:c.2354T>A	XP_011539515.1:p.Val785Asp
XM_011541214.1:c.2357T>A	XP_011539516.1:p.Val786Asp
XM_011541215.1:c.2246T>A	XP_011539517.1:p.Val749Asp
XM_011541216.1:c.2357T>A	XP_011539518.1:p.Val786Asp
XM_011541217.1:c.2357T>A	XP_011539519.1:p.Val786Asp
XM_011541218.1:c.2357T>A	XP_011539520.1:p.Val786Asp
XM_011541219.1:c.2303T>A	XP_011539521.1:p.Val768Asp
XM_011541220.1:c.2357T>A	XP_011539522.1:p.Val786Asp
XR_946604.1:n.2395T>A
XR_946605.1:n.2234T>A
XM_006710563.3:c.2357T>A	XP_006710626.1:p.Val786Asp
XM_011541216.2:c.2357T>A	XP_011539518.1:p.Val786Asp
XM_011541217.2:c.2357T>A	XP_011539519.1:p.Val786Asp
XM_011541218.2:c.2357T>A	XP_011539520.1:p.Val786Asp
XM_017000996.1:c.2354T>A	XP_016856485.1:p.Val785Asp
XM_017000997.1:c.2357T>A	XP_016856486.1:p.Val786Asp
XM_017000998.1:c.2357T>A	XP_016856487.1:p.Val786Asp
XM_017000999.1:c.1829T>A	XP_016856488.1:p.Val610Asp
XM_017001000.2:c.1829T>A	XP_016856489.1:p.Val610Asp
XM_017001001.1:c.1559T>A	XP_016856490.1:p.Val520Asp
XM_017001002.1:c.2357T>A	XP_016856491.1:p.Val786Asp
XM_017001003.1:c.818T>A	XP_016856492.1:p.Val273Asp
XR_001737114.1:n.2395T>A
XR_001737115.1:n.2395T>A
NM_015102.5:c.2357T>A MANE Select	NP_055917.1:p.Val786Asp
NM_001291593.2:c.818T>A	NP_001278522.1:p.Val273Asp
NM_001291594.2:c.821T>A	NP_001278523.1:p.Val274Asp
NR_111987.2:n.2574T>A