Canonical Allele Identifier: CA2673456117

Gene: NPR3

Linked Data

• gnomAD v4: 5-32711847-CCGGTGGCGGTGGCGTTGGCGG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.32711851_32711871del , CM000667.2:g.32711851_32711871del	GRCh38
NC_000005.9:g.32711957_32711977del , CM000667.1:g.32711957_32711977del	GRCh37
NC_000005.8:g.32747714_32747734del	NCBI36
NG_028162.1:g.6215_6235del
NG_028162.2:g.27776_27796del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265074.13:c.75_95del MANE Select	ENSP00000265074.8:p.Gly26_Gly32del
ENST00000265074.12:c.75_95del	ENSP00000265074.8:p.Gly26_Gly32del
ENST00000326958.5:c.121+1068_121+1088del	ENSP00000318340.2:n.121+1068_121+1088del
ENST00000415167.2:c.75_95del	ENSP00000398028.2:p.Gly26_Gly32del
ENST00000434067.6:c.121+1068_121+1088del	ENSP00000388408.2:n.121+1068_121+1088del
ENST00000506712.1:n.130+1068_130+1088del
ENST00000509104.5:c.101-12847_101-12827del	ENSP00000425325.1:n.101-12847_101-12827del
NM_000908.3:c.75_95del	NP_000899.1:p.Gly26_Gly32del
NM_001204375.1:c.75_95del	NP_001191304.1:p.Gly26_Gly32del
NM_001204376.1:c.121+1068_121+1088del	NP_001191305.1:n.121+1068_121+1088del
XM_005248309.1:c.121+1068_121+1088del	XP_005248366.1:n.121+1068_121+1088del
XM_005248310.2:c.75_95del	XP_005248367.1:p.Gly26_Gly32del
XM_011514047.1:c.101-12847_101-12827del	XP_011512349.1:n.101-12847_101-12827del
XM_011514048.1:c.50-12847_50-12827del	XP_011512350.1:n.50-12847_50-12827del
XM_011514049.1:c.-8-12847_-8-12827del	XP_011512351.1:n.-8-12847_-8-12827del
XM_011514050.1:c.75_95del	XP_011512352.1:p.Gly26_Gly32del
NM_001363652.1:c.121+1068_121+1088del	NP_001350581.1:n.121+1068_121+1088del
NM_001364458.1:c.50-12847_50-12827del	NP_001351387.1:n.50-12847_50-12827del
NM_001364460.1:c.121+1068_121+1088del	NP_001351389.1:n.121+1068_121+1088del
XM_011514047.2:c.101-12847_101-12827del	XP_011512349.1:n.101-12847_101-12827del
XM_011514049.3:c.-8-12847_-8-12827del	XP_011512351.1:n.-8-12847_-8-12827del
XM_011514050.2:c.75_95del	XP_011512352.1:p.Gly26_Gly32del
XM_017009492.2:c.75_95del	XP_016864981.1:p.Gly26_Gly32del
NM_001204375.2:c.75_95del MANE Select	NP_001191304.1:p.Gly26_Gly32del
NM_000908.4:c.75_95del	NP_000899.1:p.Gly26_Gly32del
NM_001363652.2:c.121+1068_121+1088del	NP_001350581.1:n.121+1068_121+1088del
NM_001364458.2:c.50-12847_50-12827del	NP_001351387.1:n.50-12847_50-12827del
NM_001364460.2:c.121+1068_121+1088del	NP_001351389.1:n.121+1068_121+1088del
NM_001204376.2:c.121+1068_121+1088del	NP_001191305.1:n.121+1068_121+1088del