Canonical Allele Identifier: CA348093020
Community Standard Title: NM_001128178.3(NPHP1):c.415G>T (p.Glu139Ter)
Gene: NPHP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.110169913C>A , CM000664.2:g.110169913C>A GRCh38
NC_000002.11:g.110927490C>A , CM000664.1:g.110927490C>A GRCh37
NC_000002.10:g.110284779C>A NCBI36
NG_008287.1:g.40150G>T

Transcript Alleles

HGVS Amino-acid Change
NM_001128178.3:c.415G>T MANE Select NP_001121650.1:p.Glu139Ter
ENST00000445609.7:c.415G>T MANE Select ENSP00000389879.3:p.Glu139Ter
NM_000272.3:c.415G>T NP_000263.2:p.Glu139Ter
NM_000272.4:c.415G>T NP_000263.2:p.Glu139Ter
NM_000272.5:c.415G>T NP_000263.2:p.Glu139Ter
NM_001128178.1:c.415G>T NP_001121650.1:p.Glu139Ter
NM_001128179.1:c.229G>T NP_001121651.1:p.Glu77Ter
NM_001128179.2:c.229G>T NP_001121651.1:p.Glu77Ter
NM_001128179.3:c.229G>T NP_001121651.1:p.Glu77Ter
NM_001374256.1:c.415G>T NP_001361185.1:p.Glu139Ter
NM_001374257.1:c.415G>T NP_001361186.1:p.Glu139Ter
NM_207181.2:c.415G>T NP_997064.2:p.Glu139Ter
NM_207181.3:c.415G>T NP_997064.2:p.Glu139Ter
NM_207181.4:c.415G>T NP_997064.2:p.Glu139Ter
ENST00000316534.8:c.415G>T ENSP00000313169.4:p.Glu139Ter
ENST00000355301.8:c.229G>T ENSP00000347452.4:p.Glu77Ter
ENST00000393272.7:c.415G>T ENSP00000376953.3:p.Glu139Ter
ENST00000417665.5:c.415G>T ENSP00000402176.1:p.Glu139Ter
ENST00000445609.6:c.415G>T ENSP00000389879.2:p.Glu139Ter
ENST00000461707.5:n.448G>T
ENST00000496524.5:n.464G>T
ENST00000674677.1:c.346G>T ENSP00000502265.1:p.Glu116Ter
ENST00000675067.1:c.-1939G>T ENSP00000502817.1:n.-1939G>T
ENST00000675356.1:n.454G>T
ENST00000675752.1:n.448G>T
ENST00000676028.1:c.415G>T ENSP00000502639.1:p.Glu139Ter
ENST00000676053.1:c.229G>T ENSP00000502475.1:p.Glu77Ter
ENST00000676165.1:n.454G>T
ENST00000676258.1:n.1506G>T
XM_005263675.1:c.415G>T XP_005263732.1:p.Glu139Ter
XM_005263676.1:c.415G>T XP_005263733.1:p.Glu139Ter
XM_005263677.1:c.415G>T XP_005263734.1:p.Glu139Ter
XM_005263678.2:c.415G>T XP_005263735.1:p.Glu139Ter
XM_005263679.1:c.415G>T XP_005263736.1:p.Glu139Ter
XM_006712551.1:c.415G>T XP_006712614.1:p.Glu139Ter
XM_006712552.2:c.415G>T XP_006712615.1:p.Glu139Ter
XM_011511244.1:c.415G>T XP_011509546.1:p.Glu139Ter
XM_017004218.1:c.415G>T XP_016859707.1:p.Glu139Ter