Canonical Allele Identifier: CA1537620237

Gene: NPR3

Linked Data

• dbSNP Id: rs1738259019

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.32711878_32711880dup , CM000667.2:g.32711878_32711880dup	GRCh38
NC_000005.9:g.32711984_32711986dup , CM000667.1:g.32711984_32711986dup	GRCh37
NC_000005.8:g.32747741_32747743dup	NCBI36
NG_028162.1:g.6242_6244dup
NG_028162.2:g.27803_27805dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265074.13:c.102_104dup MANE Select	ENSP00000265074.8:p.Gly35_Ala36insGly
ENST00000265074.12:c.102_104dup	ENSP00000265074.8:p.Gly35_Ala36insGly
ENST00000326958.5:c.121+1095_121+1097dup	ENSP00000318340.2:n.121+1095_121+1097dup
ENST00000415167.2:c.102_104dup	ENSP00000398028.2:p.Gly35_Ala36insGly
ENST00000434067.6:c.121+1095_121+1097dup	ENSP00000388408.2:n.121+1095_121+1097dup
ENST00000506712.1:n.130+1095_130+1097dup
ENST00000509104.5:c.101-12820_101-12818dup	ENSP00000425325.1:n.101-12820_101-12818dup
NM_000908.3:c.102_104dup	NP_000899.1:p.Gly35_Ala36insGly
NM_001204375.1:c.102_104dup	NP_001191304.1:p.Gly35_Ala36insGly
NM_001204376.1:c.121+1095_121+1097dup	NP_001191305.1:n.121+1095_121+1097dup
XM_005248309.1:c.121+1095_121+1097dup	XP_005248366.1:n.121+1095_121+1097dup
XM_005248310.2:c.102_104dup	XP_005248367.1:p.Gly35_Ala36insGly
XM_011514047.1:c.101-12820_101-12818dup	XP_011512349.1:n.101-12820_101-12818dup
XM_011514048.1:c.50-12820_50-12818dup	XP_011512350.1:n.50-12820_50-12818dup
XM_011514049.1:c.-8-12820_-8-12818dup	XP_011512351.1:n.-8-12820_-8-12818dup
XM_011514050.1:c.102_104dup	XP_011512352.1:p.Gly35_Ala36insGly
NM_001363652.1:c.121+1095_121+1097dup	NP_001350581.1:n.121+1095_121+1097dup
NM_001364458.1:c.50-12820_50-12818dup	NP_001351387.1:n.50-12820_50-12818dup
NM_001364460.1:c.121+1095_121+1097dup	NP_001351389.1:n.121+1095_121+1097dup
XM_011514047.2:c.101-12820_101-12818dup	XP_011512349.1:n.101-12820_101-12818dup
XM_011514049.3:c.-8-12820_-8-12818dup	XP_011512351.1:n.-8-12820_-8-12818dup
XM_011514050.2:c.102_104dup	XP_011512352.1:p.Gly35_Ala36insGly
XM_017009492.2:c.102_104dup	XP_016864981.1:p.Gly35_Ala36insGly
NM_001204375.2:c.102_104dup MANE Select	NP_001191304.1:p.Gly35_Ala36insGly
NM_000908.4:c.102_104dup	NP_000899.1:p.Gly35_Ala36insGly
NM_001363652.2:c.121+1095_121+1097dup	NP_001350581.1:n.121+1095_121+1097dup
NM_001364458.2:c.50-12820_50-12818dup	NP_001351387.1:n.50-12820_50-12818dup
NM_001364460.2:c.121+1095_121+1097dup	NP_001351389.1:n.121+1095_121+1097dup
NM_001204376.2:c.121+1095_121+1097dup	NP_001191305.1:n.121+1095_121+1097dup