Canonical Allele Identifier: CA338047265

Gene: NPHP4

Linked Data

• MyVariant Identifiers: chr1:g.5923348A>T (hg19) ; chr1:g.5863288A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.5863288A>T , CM000663.2:g.5863288A>T	GRCh38
NC_000001.10:g.5923348A>T , CM000663.1:g.5923348A>T	GRCh37
NC_000001.9:g.5845935A>T	NCBI36
NG_011724.2:g.134184T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378156.9:c.4258T>A MANE Select	ENSP00000367398.4:p.Cys1420Ser
ENST00000378156.8:c.4258T>A	ENSP00000367398.4:p.Cys1420Ser
ENST00000378161.5:n.3893T>A
ENST00000378169.7:c.*3159T>A	ENSP00000367411.3:n.*3159T>A
ENST00000460696.1:n.3490T>A
ENST00000478423.6:n.3990T>A
ENST00000489180.6:c.*2069T>A	ENSP00000423747.1:n.*2069T>A
NM_001291593.1:c.2719T>A	NP_001278522.1:p.Cys907Ser
NM_001291594.1:c.2722T>A	NP_001278523.1:p.Cys908Ser
NM_015102.4:c.4258T>A	NP_055917.1:p.Cys1420Ser
NR_111987.1:n.5073T>A
XM_006710563.2:c.4258T>A	XP_006710626.1:p.Cys1420Ser
XM_006710565.2:c.4258T>A	XP_006710628.1:p.Cys1420Ser
XM_011541213.1:c.4255T>A	XP_011539515.1:p.Cys1419Ser
XM_011541214.1:c.4216T>A	XP_011539516.1:p.Cys1406Ser
XM_011541215.1:c.4147T>A	XP_011539517.1:p.Cys1383Ser
XM_011541216.1:c.4258T>A	XP_011539518.1:p.Cys1420Ser
XM_011541217.1:c.4258T>A	XP_011539519.1:p.Cys1420Ser
XM_011541218.1:c.4258T>A	XP_011539520.1:p.Cys1420Ser
XM_011541219.1:c.4204T>A	XP_011539521.1:p.Cys1402Ser
XM_006710563.3:c.4258T>A	XP_006710626.1:p.Cys1420Ser
XM_011541216.2:c.4258T>A	XP_011539518.1:p.Cys1420Ser
XM_011541217.2:c.4258T>A	XP_011539519.1:p.Cys1420Ser
XM_011541218.2:c.4258T>A	XP_011539520.1:p.Cys1420Ser
XM_017000996.1:c.4213T>A	XP_016856485.1:p.Cys1405Ser
XM_017000997.1:c.4258T>A	XP_016856486.1:p.Cys1420Ser
XM_017000999.1:c.3730T>A	XP_016856488.1:p.Cys1244Ser
XM_017001000.2:c.3730T>A	XP_016856489.1:p.Cys1244Ser
XM_017001001.1:c.3460T>A	XP_016856490.1:p.Cys1154Ser
XM_017001003.1:c.2719T>A	XP_016856492.1:p.Cys907Ser
XR_001737114.1:n.4124T>A
XR_001737115.1:n.4109T>A
NM_015102.5:c.4258T>A MANE Select	NP_055917.1:p.Cys1420Ser
NM_001291593.2:c.2719T>A	NP_001278522.1:p.Cys907Ser
NM_001291594.2:c.2722T>A	NP_001278523.1:p.Cys908Ser
NR_111987.2:n.5025T>A