Canonical Allele Identifier: CA1537676175

Gene: NPR3

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.32786283A= , CM000667.2:g.32786283A=	GRCh38
NC_000005.9:g.32786389A= , CM000667.1:g.32786389A=	GRCh37
NC_000005.8:g.32822146A=	NCBI36
NG_028162.1:g.80647A=
NG_028162.2:g.102208A=

Transcript Alleles

HGVS	Amino-acid Change
NM_001204375.2:c.1564A= MANE Select	NP_001191304.1:p.Asn522=
ENST00000265074.13:c.1564A= MANE Select	ENSP00000265074.8:p.Asn522=
NM_000908.3:c.1561A=	NP_000899.1:p.Asn521=
NM_000908.4:c.1561A=	NP_000899.1:p.Asn521=
NM_001204375.1:c.1564A=	NP_001191304.1:p.Asn522=
NM_001204376.1:c.913A=	NP_001191305.1:p.Asn305=
NM_001204376.2:c.913A=	NP_001191305.1:p.Asn305=
NM_001363652.1:c.916A=	NP_001350581.1:p.Asn306=
NM_001363652.2:c.916A=	NP_001350581.1:p.Asn306=
NM_001364458.1:c.844A=	NP_001351387.1:p.Asn282=
NM_001364458.2:c.844A=	NP_001351387.1:p.Asn282=
NM_001364460.1:c.793A=	NP_001351389.1:p.Asn265=
NM_001364460.2:c.793A=	NP_001351389.1:p.Asn265=
ENST00000265074.12:c.1564A=	ENSP00000265074.8:p.Asn522=
ENST00000326958.5:c.913A=	ENSP00000318340.2:p.Asn305=
ENST00000415167.2:c.1561A=	ENSP00000398028.2:p.Asn521=
ENST00000434067.6:c.916A=	ENSP00000388408.2:p.Asn306=
XM_005248309.1:c.916A=	XP_005248366.1:p.Asn306=
XM_011514047.1:c.895A=	XP_011512349.1:p.Asn299=
XM_011514047.2:c.895A=	XP_011512349.1:p.Asn299=
XM_011514048.1:c.844A=	XP_011512350.1:p.Asn282=
XM_011514049.1:c.787A=	XP_011512351.1:p.Asn263=
XM_011514049.3:c.787A=	XP_011512351.1:p.Asn263=
XM_017009492.2:c.1441A=	XP_016864981.1:p.Asn481=