Canonical Allele Identifier: CA809906835

Gene: NPR3

Linked Data

• dbSNP Id: rs1287905079
• gnomAD v3: 5-32719594-C-T
• gnomAD v4: 5-32719594-C-T
• MyVariant Identifiers: chr5:g.32719700C>T (hg19) ; chr5:g.32719594C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.32719594C>T , CM000667.2:g.32719594C>T	GRCh38
NC_000005.9:g.32719700C>T , CM000667.1:g.32719700C>T	GRCh37
NC_000005.8:g.32755457C>T	NCBI36
NG_028162.1:g.13958C>T
NG_028162.2:g.35519C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000265074.13:c.770-5104C>T MANE Select	ENSP00000265074.8:n.770-5104C>T
ENST00000265074.12:c.770-5104C>T	ENSP00000265074.8:n.770-5104C>T
ENST00000326958.5:c.122-5104C>T	ENSP00000318340.2:n.122-5104C>T
ENST00000415167.2:c.770-5104C>T	ENSP00000398028.2:n.770-5104C>T
ENST00000434067.6:c.122-5104C>T	ENSP00000388408.2:n.122-5104C>T
ENST00000506712.1:n.131-5104C>T
ENST00000509104.5:c.101-5104C>T	ENSP00000425325.1:n.101-5104C>T
NM_000908.3:c.770-5104C>T	NP_000899.1:n.770-5104C>T
NM_001204375.1:c.770-5104C>T	NP_001191304.1:n.770-5104C>T
NM_001204376.1:c.122-5104C>T	NP_001191305.1:n.122-5104C>T
XM_005248309.1:c.122-5104C>T	XP_005248366.1:n.122-5104C>T
XM_011514047.1:c.101-5104C>T	XP_011512349.1:n.101-5104C>T
XM_011514048.1:c.50-5104C>T	XP_011512350.1:n.50-5104C>T
XM_011514049.1:c.-8-5104C>T	XP_011512351.1:n.-8-5104C>T
NM_001363652.1:c.122-5104C>T	NP_001350581.1:n.122-5104C>T
NM_001364458.1:c.50-5104C>T	NP_001351387.1:n.50-5104C>T
NM_001364460.1:c.121+8811C>T	NP_001351389.1:n.121+8811C>T
XM_011514047.2:c.101-5104C>T	XP_011512349.1:n.101-5104C>T
XM_011514049.3:c.-8-5104C>T	XP_011512351.1:n.-8-5104C>T
XM_017009492.2:c.769+7049C>T	XP_016864981.1:n.769+7049C>T
NM_001204375.2:c.770-5104C>T MANE Select	NP_001191304.1:n.770-5104C>T
NM_000908.4:c.770-5104C>T	NP_000899.1:n.770-5104C>T
NM_001363652.2:c.122-5104C>T	NP_001350581.1:n.122-5104C>T
NM_001364458.2:c.50-5104C>T	NP_001351387.1:n.50-5104C>T
NM_001364460.2:c.121+8811C>T	NP_001351389.1:n.121+8811C>T
NM_001204376.2:c.122-5104C>T	NP_001191305.1:n.122-5104C>T