Canonical Allele Identifier: CA1278852895
Gene: NPHP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.110201449G= , CM000664.2:g.110201449G= GRCh38
NC_000002.11:g.110959026G= , CM000664.1:g.110959026G= GRCh37
NC_000002.10:g.110316315G= NCBI36
NG_008287.1:g.8614C=

Transcript Alleles

HGVS Amino-acid Change
NM_001128178.3:c.115C= MANE Select NP_001121650.1:p.Pro39=
ENST00000445609.7:c.115C= MANE Select ENSP00000389879.3:p.Pro39=
NM_000272.3:c.115C= NP_000263.2:p.Pro39=
NM_000272.4:c.115C= NP_000263.2:p.Pro39=
NM_000272.5:c.115C= NP_000263.2:p.Pro39=
NM_001128178.1:c.115C= NP_001121650.1:p.Pro39=
NM_001128179.1:c.115C= NP_001121651.1:p.Pro39=
NM_001128179.2:c.115C= NP_001121651.1:p.Pro39=
NM_001128179.3:c.115C= NP_001121651.1:p.Pro39=
NM_001374256.1:c.115C= NP_001361185.1:p.Pro39=
NM_001374257.1:c.115C= NP_001361186.1:p.Pro39=
NM_207181.2:c.115C= NP_997064.2:p.Pro39=
NM_207181.3:c.115C= NP_997064.2:p.Pro39=
NM_207181.4:c.115C= NP_997064.2:p.Pro39=
ENST00000316534.8:c.115C= ENSP00000313169.4:p.Pro39=
ENST00000355301.8:c.115C= ENSP00000347452.4:p.Pro39=
ENST00000393272.7:c.115C= ENSP00000376953.3:p.Pro39=
ENST00000417665.5:c.115C= ENSP00000402176.1:p.Pro39=
ENST00000418527.1:c.115C= ENSP00000412351.1:p.Pro39=
ENST00000445609.6:c.115C= ENSP00000389879.2:p.Pro39=
ENST00000449600.1:c.215C=
ENST00000461707.5:n.148C=
ENST00000496524.5:n.164C=
ENST00000674677.1:c.46C= ENSP00000502265.1:p.Pro16=
ENST00000675067.1:c.-2211+3451C= ENSP00000502817.1:n.-2211+3451C=
ENST00000675356.1:n.154C=
ENST00000675752.1:n.130C=
ENST00000676028.1:c.115C= ENSP00000502639.1:p.Pro39=
ENST00000676053.1:c.115C= ENSP00000502475.1:p.Pro39=
ENST00000676165.1:n.154C=
ENST00000676258.1:n.130C=
XM_005263675.1:c.115C= XP_005263732.1:p.Pro39=
XM_005263676.1:c.115C= XP_005263733.1:p.Pro39=
XM_005263677.1:c.115C= XP_005263734.1:p.Pro39=
XM_005263678.2:c.115C= XP_005263735.1:p.Pro39=
XM_005263679.1:c.115C= XP_005263736.1:p.Pro39=
XM_006712551.1:c.115C= XP_006712614.1:p.Pro39=
XM_006712552.2:c.115C= XP_006712615.1:p.Pro39=
XM_011511244.1:c.115C= XP_011509546.1:p.Pro39=
XM_017004218.1:c.115C= XP_016859707.1:p.Pro39=