Canonical Allele Identifier: CA1537674783

Gene: NPR3

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.32784801G= , CM000667.2:g.32784801G=	GRCh38
NC_000005.9:g.32784907G= , CM000667.1:g.32784907G=	GRCh37
NC_000005.8:g.32820664G=	NCBI36
NG_028162.1:g.79165G=
NG_028162.2:g.100726G=

Transcript Alleles

HGVS	Amino-acid Change
NM_001204375.2:c.1432G= MANE Select	NP_001191304.1:p.Gly478=
ENST00000265074.13:c.1432G= MANE Select	ENSP00000265074.8:p.Gly478=
NM_000908.3:c.1429G=	NP_000899.1:p.Gly477=
NM_000908.4:c.1429G=	NP_000899.1:p.Gly477=
NM_001204375.1:c.1432G=	NP_001191304.1:p.Gly478=
NM_001204376.1:c.781G=	NP_001191305.1:p.Gly261=
NM_001204376.2:c.781G=	NP_001191305.1:p.Gly261=
NM_001363652.1:c.784G=	NP_001350581.1:p.Gly262=
NM_001363652.2:c.784G=	NP_001350581.1:p.Gly262=
NM_001364458.1:c.712G=	NP_001351387.1:p.Gly238=
NM_001364458.2:c.712G=	NP_001351387.1:p.Gly238=
NM_001364460.1:c.661G=	NP_001351389.1:p.Gly221=
NM_001364460.2:c.661G=	NP_001351389.1:p.Gly221=
ENST00000265074.12:c.1432G=	ENSP00000265074.8:p.Gly478=
ENST00000326958.5:c.781G=	ENSP00000318340.2:p.Gly261=
ENST00000415167.2:c.1429G=	ENSP00000398028.2:p.Gly477=
ENST00000434067.6:c.784G=	ENSP00000388408.2:p.Gly262=
XM_005248309.1:c.784G=	XP_005248366.1:p.Gly262=
XM_011514047.1:c.763G=	XP_011512349.1:p.Gly255=
XM_011514047.2:c.763G=	XP_011512349.1:p.Gly255=
XM_011514048.1:c.712G=	XP_011512350.1:p.Gly238=
XM_011514049.1:c.655G=	XP_011512351.1:p.Gly219=
XM_011514049.3:c.655G=	XP_011512351.1:p.Gly219=
XM_017009492.2:c.1309G=	XP_016864981.1:p.Gly437=