Canonical Allele Identifier: CA1537613843
Gene: NPR3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.32714164C= , CM000667.2:g.32714164C= GRCh38
NC_000005.9:g.32714270C= , CM000667.1:g.32714270C= GRCh37
NC_000005.8:g.32750027C= NCBI36
NG_028162.1:g.8528C=
NG_028162.2:g.30089C=

Transcript Alleles

HGVS Amino-acid Change
NM_001204375.2:c.769+1619C= MANE Select NP_001191304.1:n.769+1619C=
ENST00000265074.13:c.769+1619C= MANE Select ENSP00000265074.8:n.769+1619C=
NM_000908.3:c.769+1619C= NP_000899.1:n.769+1619C=
NM_000908.4:c.769+1619C= NP_000899.1:n.769+1619C=
NM_001204375.1:c.769+1619C= NP_001191304.1:n.769+1619C=
NM_001204376.1:c.121+3381C= NP_001191305.1:n.121+3381C=
NM_001204376.2:c.121+3381C= NP_001191305.1:n.121+3381C=
NM_001363652.1:c.121+3381C= NP_001350581.1:n.121+3381C=
NM_001363652.2:c.121+3381C= NP_001350581.1:n.121+3381C=
NM_001364458.1:c.50-10534C= NP_001351387.1:n.50-10534C=
NM_001364458.2:c.50-10534C= NP_001351387.1:n.50-10534C=
NM_001364460.1:c.121+3381C= NP_001351389.1:n.121+3381C=
NM_001364460.2:c.121+3381C= NP_001351389.1:n.121+3381C=
ENST00000265074.12:c.769+1619C= ENSP00000265074.8:n.769+1619C=
ENST00000326958.5:c.121+3381C= ENSP00000318340.2:n.121+3381C=
ENST00000415167.2:c.769+1619C= ENSP00000398028.2:n.769+1619C=
ENST00000434067.6:c.121+3381C= ENSP00000388408.2:n.121+3381C=
ENST00000506712.1:n.130+3381C=
ENST00000507141.1:c.215+1619C=
ENST00000509104.5:c.101-10534C= ENSP00000425325.1:n.101-10534C=
XM_005248309.1:c.121+3381C= XP_005248366.1:n.121+3381C=
XM_005248310.2:c.*938C= XP_005248367.1:n.*938C=
XM_011514047.1:c.101-10534C= XP_011512349.1:n.101-10534C=
XM_011514047.2:c.101-10534C= XP_011512349.1:n.101-10534C=
XM_011514048.1:c.50-10534C= XP_011512350.1:n.50-10534C=
XM_011514049.1:c.-8-10534C= XP_011512351.1:n.-8-10534C=
XM_011514049.3:c.-8-10534C= XP_011512351.1:n.-8-10534C=
XM_011514050.1:c.769+1619C= XP_011512352.1:n.769+1619C=
XM_011514050.2:c.769+1619C= XP_011512352.1:n.769+1619C=
XM_017009492.2:c.769+1619C= XP_016864981.1:n.769+1619C=