Canonical Allele Identifier: CA1537662718

Gene: NPR3

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.32768754C= , CM000667.2:g.32768754C=	GRCh38
NC_000005.9:g.32768860C= , CM000667.1:g.32768860C=	GRCh37
NC_000005.8:g.32804617C=	NCBI36
NG_028162.1:g.63118C=
NG_028162.2:g.84679C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265074.13:c.1060-5954C= MANE Select	ENSP00000265074.8:n.1060-5954C=
ENST00000265074.12:c.1060-5954C=	ENSP00000265074.8:n.1060-5954C=
ENST00000326958.5:c.412-5954C=	ENSP00000318340.2:n.412-5954C=
ENST00000415167.2:c.1060-5954C=	ENSP00000398028.2:n.1060-5954C=
ENST00000434067.6:c.412-5954C=	ENSP00000388408.2:n.412-5954C=
ENST00000506712.1:n.421-5954C=
ENST00000509104.5:c.391-5954C=	ENSP00000425325.1:n.391-5954C=
NM_000908.3:c.1060-5954C=	NP_000899.1:n.1060-5954C=
NM_001204375.1:c.1060-5954C=	NP_001191304.1:n.1060-5954C=
NM_001204376.1:c.412-5954C=	NP_001191305.1:n.412-5954C=
XM_005248309.1:c.412-5954C=	XP_005248366.1:n.412-5954C=
XM_011514047.1:c.391-5954C=	XP_011512349.1:n.391-5954C=
XM_011514048.1:c.340-5954C=	XP_011512350.1:n.340-5954C=
XM_011514049.1:c.283-5954C=	XP_011512351.1:n.283-5954C=
NM_001363652.1:c.412-5954C=	NP_001350581.1:n.412-5954C=
NM_001364458.1:c.340-5954C=	NP_001351387.1:n.340-5954C=
NM_001364460.1:c.289-5954C=	NP_001351389.1:n.289-5954C=
XM_011514047.2:c.391-5954C=	XP_011512349.1:n.391-5954C=
XM_011514049.3:c.283-5954C=	XP_011512351.1:n.283-5954C=
XM_017009492.2:c.937-5954C=	XP_016864981.1:n.937-5954C=
NM_001204375.2:c.1060-5954C= MANE Select	NP_001191304.1:n.1060-5954C=
NM_000908.4:c.1060-5954C=	NP_000899.1:n.1060-5954C=
NM_001363652.2:c.412-5954C=	NP_001350581.1:n.412-5954C=
NM_001364458.2:c.340-5954C=	NP_001351387.1:n.340-5954C=
NM_001364460.2:c.289-5954C=	NP_001351389.1:n.289-5954C=
NM_001204376.2:c.412-5954C=	NP_001191305.1:n.412-5954C=