Canonical Allele Identifier: CA2838528312

Gene: NPR3

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.32768591C>A , CM000667.2:g.32768591C>A	GRCh38
NC_000005.9:g.32768697C>A , CM000667.1:g.32768697C>A	GRCh37
NC_000005.8:g.32804454C>A	NCBI36
NG_028162.1:g.62955C>A
NG_028162.2:g.84516C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265074.13:c.1060-6117C>A MANE Select	ENSP00000265074.8:n.1060-6117C>A
ENST00000265074.12:c.1060-6117C>A	ENSP00000265074.8:n.1060-6117C>A
ENST00000326958.5:c.412-6117C>A	ENSP00000318340.2:n.412-6117C>A
ENST00000415167.2:c.1060-6117C>A	ENSP00000398028.2:n.1060-6117C>A
ENST00000434067.6:c.412-6117C>A	ENSP00000388408.2:n.412-6117C>A
ENST00000506712.1:n.421-6117C>A
ENST00000509104.5:c.391-6117C>A	ENSP00000425325.1:n.391-6117C>A
NM_000908.3:c.1060-6117C>A	NP_000899.1:n.1060-6117C>A
NM_001204375.1:c.1060-6117C>A	NP_001191304.1:n.1060-6117C>A
NM_001204376.1:c.412-6117C>A	NP_001191305.1:n.412-6117C>A
XM_005248309.1:c.412-6117C>A	XP_005248366.1:n.412-6117C>A
XM_011514047.1:c.391-6117C>A	XP_011512349.1:n.391-6117C>A
XM_011514048.1:c.340-6117C>A	XP_011512350.1:n.340-6117C>A
XM_011514049.1:c.283-6117C>A	XP_011512351.1:n.283-6117C>A
NM_001363652.1:c.412-6117C>A	NP_001350581.1:n.412-6117C>A
NM_001364458.1:c.340-6117C>A	NP_001351387.1:n.340-6117C>A
NM_001364460.1:c.289-6117C>A	NP_001351389.1:n.289-6117C>A
XM_011514047.2:c.391-6117C>A	XP_011512349.1:n.391-6117C>A
XM_011514049.3:c.283-6117C>A	XP_011512351.1:n.283-6117C>A
XM_017009492.2:c.937-6117C>A	XP_016864981.1:n.937-6117C>A
NM_001204375.2:c.1060-6117C>A MANE Select	NP_001191304.1:n.1060-6117C>A
NM_000908.4:c.1060-6117C>A	NP_000899.1:n.1060-6117C>A
NM_001363652.2:c.412-6117C>A	NP_001350581.1:n.412-6117C>A
NM_001364458.2:c.340-6117C>A	NP_001351387.1:n.340-6117C>A
NM_001364460.2:c.289-6117C>A	NP_001351389.1:n.289-6117C>A
NM_001204376.2:c.412-6117C>A	NP_001191305.1:n.412-6117C>A