Canonical Allele Identifier: CA338049154

Gene: NPHP4

Linked Data

• MyVariant Identifiers: chr1:g.5924054C>A (hg19) ; chr1:g.5863994C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.5863994C>A , CM000663.2:g.5863994C>A	GRCh38
NC_000001.10:g.5924054C>A , CM000663.1:g.5924054C>A	GRCh37
NC_000001.9:g.5846641C>A	NCBI36
NG_011724.2:g.133478G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378156.9:c.4036G>T MANE Select	ENSP00000367398.4:p.Val1346Phe
ENST00000378156.8:c.4036G>T	ENSP00000367398.4:p.Val1346Phe
ENST00000378161.5:n.3187G>T
ENST00000378169.7:c.*2937G>T	ENSP00000367411.3:n.*2937G>T
ENST00000460696.1:n.2784G>T
ENST00000478423.6:n.3768G>T
ENST00000489180.6:c.*1847G>T	ENSP00000423747.1:n.*1847G>T
NM_001291593.1:c.2497G>T	NP_001278522.1:p.Val833Phe
NM_001291594.1:c.2500G>T	NP_001278523.1:p.Val834Phe
NM_015102.4:c.4036G>T	NP_055917.1:p.Val1346Phe
NR_111987.1:n.4851G>T
XM_006710563.2:c.4036G>T	XP_006710626.1:p.Val1346Phe
XM_006710565.2:c.4036G>T	XP_006710628.1:p.Val1346Phe
XM_011541213.1:c.4033G>T	XP_011539515.1:p.Val1345Phe
XM_011541214.1:c.3994G>T	XP_011539516.1:p.Val1332Phe
XM_011541215.1:c.3925G>T	XP_011539517.1:p.Val1309Phe
XM_011541216.1:c.4036G>T	XP_011539518.1:p.Val1346Phe
XM_011541217.1:c.4036G>T	XP_011539519.1:p.Val1346Phe
XM_011541218.1:c.4036G>T	XP_011539520.1:p.Val1346Phe
XM_011541219.1:c.3982G>T	XP_011539521.1:p.Val1328Phe
XM_006710563.3:c.4036G>T	XP_006710626.1:p.Val1346Phe
XM_011541216.2:c.4036G>T	XP_011539518.1:p.Val1346Phe
XM_011541217.2:c.4036G>T	XP_011539519.1:p.Val1346Phe
XM_011541218.2:c.4036G>T	XP_011539520.1:p.Val1346Phe
XM_017000996.1:c.3991G>T	XP_016856485.1:p.Val1331Phe
XM_017000997.1:c.4036G>T	XP_016856486.1:p.Val1346Phe
XM_017000999.1:c.3508G>T	XP_016856488.1:p.Val1170Phe
XM_017001000.2:c.3508G>T	XP_016856489.1:p.Val1170Phe
XM_017001001.1:c.3238G>T	XP_016856490.1:p.Val1080Phe
XM_017001003.1:c.2497G>T	XP_016856492.1:p.Val833Phe
XR_001737114.1:n.3902G>T
XR_001737115.1:n.3887G>T
NM_015102.5:c.4036G>T MANE Select	NP_055917.1:p.Val1346Phe
NM_001291593.2:c.2497G>T	NP_001278522.1:p.Val833Phe
NM_001291594.2:c.2500G>T	NP_001278523.1:p.Val834Phe
NR_111987.2:n.4803G>T