Canonical Allele Identifier: CA1537659397

Gene: NPR3

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.32748717_32748732delinsGGGAGGGGAATGAATT , CM000667.2:g.32748717_32748732delinsGGGAGGGGAATGAATT	GRCh38
NC_000005.9:g.32748823_32748838delinsGGGAGGGGAATGAATT , CM000667.1:g.32748823_32748838delinsGGGAGGGGAATGAATT	GRCh37
NC_000005.8:g.32784580_32784595delinsGGGAGGGGAATGAATT	NCBI36
NG_028162.1:g.43081_43096delinsGGGAGGGGAATGAATT
NG_028162.2:g.64642_64657delinsGGGAGGGGAATGAATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265074.13:c.1059+9687_1059+9702delinsGGGAGGGGAATGAATT MANE Select	ENSP00000265074.8:n.1059+9687_1059+9702delinsGGGAGGGGAATGAATT...
ENST00000265074.12:c.1059+9687_1059+9702delinsGGGAGGGGAATGAATT	ENSP00000265074.8:n.1059+9687_1059+9702delinsGGGAGGGGAATGAATT...
ENST00000326958.5:c.411+9687_411+9702delinsGGGAGGGGAATGAATT	ENSP00000318340.2:n.411+9687_411+9702delinsGGGAGGGGAATGAATT
ENST00000415167.2:c.1059+9687_1059+9702delinsGGGAGGGGAATGAATT	ENSP00000398028.2:n.1059+9687_1059+9702delinsGGGAGGGGAATGAATT...
ENST00000434067.6:c.411+9687_411+9702delinsGGGAGGGGAATGAATT	ENSP00000388408.2:n.411+9687_411+9702delinsGGGAGGGGAATGAATT
ENST00000506712.1:n.420+9687_420+9702delinsGGGAGGGGAATGAATT
ENST00000509104.5:c.390+9687_390+9702delinsGGGAGGGGAATGAATT	ENSP00000425325.1:n.390+9687_390+9702delinsGGGAGGGGAATGAATT
NM_000908.3:c.1059+9687_1059+9702delinsGGGAGGGGAATGAATT	NP_000899.1:n.1059+9687_1059+9702delinsGGGAGGGGAATGAATT
NM_001204375.1:c.1059+9687_1059+9702delinsGGGAGGGGAATGAATT	NP_001191304.1:n.1059+9687_1059+9702delinsGGGAGGGGAATGAATT
NM_001204376.1:c.411+9687_411+9702delinsGGGAGGGGAATGAATT	NP_001191305.1:n.411+9687_411+9702delinsGGGAGGGGAATGAATT
XM_005248309.1:c.411+9687_411+9702delinsGGGAGGGGAATGAATT	XP_005248366.1:n.411+9687_411+9702delinsGGGAGGGGAATGAATT
XM_011514047.1:c.390+9687_390+9702delinsGGGAGGGGAATGAATT	XP_011512349.1:n.390+9687_390+9702delinsGGGAGGGGAATGAATT
XM_011514048.1:c.339+9687_339+9702delinsGGGAGGGGAATGAATT	XP_011512350.1:n.339+9687_339+9702delinsGGGAGGGGAATGAATT
XM_011514049.1:c.282+9687_282+9702delinsGGGAGGGGAATGAATT	XP_011512351.1:n.282+9687_282+9702delinsGGGAGGGGAATGAATT
NM_001363652.1:c.411+9687_411+9702delinsGGGAGGGGAATGAATT	NP_001350581.1:n.411+9687_411+9702delinsGGGAGGGGAATGAATT
NM_001364458.1:c.339+9687_339+9702delinsGGGAGGGGAATGAATT	NP_001351387.1:n.339+9687_339+9702delinsGGGAGGGGAATGAATT
NM_001364460.1:c.288+9687_288+9702delinsGGGAGGGGAATGAATT	NP_001351389.1:n.288+9687_288+9702delinsGGGAGGGGAATGAATT
XM_011514047.2:c.390+9687_390+9702delinsGGGAGGGGAATGAATT	XP_011512349.1:n.390+9687_390+9702delinsGGGAGGGGAATGAATT
XM_011514049.3:c.282+9687_282+9702delinsGGGAGGGGAATGAATT	XP_011512351.1:n.282+9687_282+9702delinsGGGAGGGGAATGAATT
XM_017009492.2:c.936+9687_936+9702delinsGGGAGGGGAATGAATT	XP_016864981.1:n.936+9687_936+9702delinsGGGAGGGGAATGAATT
NM_001204375.2:c.1059+9687_1059+9702delinsGGGAGGGGAATGAATT MANE Select	NP_001191304.1:n.1059+9687_1059+9702delinsGGGAGGGGAATGAATT
NM_000908.4:c.1059+9687_1059+9702delinsGGGAGGGGAATGAATT	NP_000899.1:n.1059+9687_1059+9702delinsGGGAGGGGAATGAATT
NM_001363652.2:c.411+9687_411+9702delinsGGGAGGGGAATGAATT	NP_001350581.1:n.411+9687_411+9702delinsGGGAGGGGAATGAATT
NM_001364458.2:c.339+9687_339+9702delinsGGGAGGGGAATGAATT	NP_001351387.1:n.339+9687_339+9702delinsGGGAGGGGAATGAATT
NM_001364460.2:c.288+9687_288+9702delinsGGGAGGGGAATGAATT	NP_001351389.1:n.288+9687_288+9702delinsGGGAGGGGAATGAATT
NM_001204376.2:c.411+9687_411+9702delinsGGGAGGGGAATGAATT	NP_001191305.1:n.411+9687_411+9702delinsGGGAGGGGAATGAATT