Canonical Allele Identifier: CA1537647912

Gene: NPR3

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.32734762A>T , CM000667.2:g.32734762A>T	GRCh38
NC_000005.9:g.32734868A>T , CM000667.1:g.32734868A>T	GRCh37
NC_000005.8:g.32770625A>T	NCBI36
NG_028162.1:g.29126A>T
NG_028162.2:g.50687A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265074.13:c.893-4102A>T MANE Select	ENSP00000265074.8:n.893-4102A>T
ENST00000265074.12:c.893-4102A>T	ENSP00000265074.8:n.893-4102A>T
ENST00000326958.5:c.245-4102A>T	ENSP00000318340.2:n.245-4102A>T
ENST00000415167.2:c.893-4102A>T	ENSP00000398028.2:n.893-4102A>T
ENST00000434067.6:c.245-4102A>T	ENSP00000388408.2:n.245-4102A>T
ENST00000506712.1:n.254-4102A>T
ENST00000509104.5:c.224-4102A>T	ENSP00000425325.1:n.224-4102A>T
NM_000908.3:c.893-4102A>T	NP_000899.1:n.893-4102A>T
NM_001204375.1:c.893-4102A>T	NP_001191304.1:n.893-4102A>T
NM_001204376.1:c.245-4102A>T	NP_001191305.1:n.245-4102A>T
XM_005248309.1:c.245-4102A>T	XP_005248366.1:n.245-4102A>T
XM_011514047.1:c.224-4102A>T	XP_011512349.1:n.224-4102A>T
XM_011514048.1:c.173-4102A>T	XP_011512350.1:n.173-4102A>T
XM_011514049.1:c.116-4102A>T	XP_011512351.1:n.116-4102A>T
NM_001363652.1:c.245-4102A>T	NP_001350581.1:n.245-4102A>T
NM_001364458.1:c.173-4102A>T	NP_001351387.1:n.173-4102A>T
NM_001364460.1:c.122-4102A>T	NP_001351389.1:n.122-4102A>T
XM_011514047.2:c.224-4102A>T	XP_011512349.1:n.224-4102A>T
XM_011514049.3:c.116-4102A>T	XP_011512351.1:n.116-4102A>T
XM_017009492.2:c.770-4102A>T	XP_016864981.1:n.770-4102A>T
NM_001204375.2:c.893-4102A>T MANE Select	NP_001191304.1:n.893-4102A>T
NM_000908.4:c.893-4102A>T	NP_000899.1:n.893-4102A>T
NM_001363652.2:c.245-4102A>T	NP_001350581.1:n.245-4102A>T
NM_001364458.2:c.173-4102A>T	NP_001351387.1:n.173-4102A>T
NM_001364460.2:c.122-4102A>T	NP_001351389.1:n.122-4102A>T
NM_001204376.2:c.245-4102A>T	NP_001191305.1:n.245-4102A>T