Canonical Allele Identifier: CA116857588

Gene: NPR3

Linked Data

• dbSNP Id: rs2270915
• MyVariant Identifiers: chr5:g.32786389A>C (hg19) ; chr5:g.32786283A>C (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000265074.13:c.1564A>C MANE Select	ENSP00000265074.8:p.Asn522His
ENST00000265074.12:c.1564A>C	ENSP00000265074.8:p.Asn522His
ENST00000326958.5:c.913A>C	ENSP00000318340.2:p.Asn305His
ENST00000415167.2:c.1561A>C	ENSP00000398028.2:p.Asn521His
ENST00000434067.6:c.916A>C	ENSP00000388408.2:p.Asn306His
NM_000908.3:c.1561A>C	NP_000899.1:p.Asn521His
NM_001204375.1:c.1564A>C	NP_001191304.1:p.Asn522His
NM_001204376.1:c.913A>C	NP_001191305.1:p.Asn305His
XM_005248309.1:c.916A>C	XP_005248366.1:p.Asn306His
XM_011514047.1:c.895A>C	XP_011512349.1:p.Asn299His
XM_011514048.1:c.844A>C	XP_011512350.1:p.Asn282His
XM_011514049.1:c.787A>C	XP_011512351.1:p.Asn263His
NM_001363652.1:c.916A>C	NP_001350581.1:p.Asn306His
NM_001364458.1:c.844A>C	NP_001351387.1:p.Asn282His
NM_001364460.1:c.793A>C	NP_001351389.1:p.Asn265His
XM_011514047.2:c.895A>C	XP_011512349.1:p.Asn299His
XM_011514049.3:c.787A>C	XP_011512351.1:p.Asn263His
XM_017009492.2:c.1441A>C	XP_016864981.1:p.Asn481His
NM_001204375.2:c.1564A>C MANE Select	NP_001191304.1:p.Asn522His
NM_000908.4:c.1561A>C	NP_000899.1:p.Asn521His
NM_001363652.2:c.916A>C	NP_001350581.1:p.Asn306His
NM_001364458.2:c.844A>C	NP_001351387.1:p.Asn282His
NM_001364460.2:c.793A>C	NP_001351389.1:p.Asn265His
NM_001204376.2:c.913A>C	NP_001191305.1:p.Asn305His