Canonical Allele Identifier: CA1537659345

Gene: NPR3

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.32748580_32748583delinsCTGG , CM000667.2:g.32748580_32748583delinsCTGG	GRCh38
NC_000005.9:g.32748686_32748689delinsCTGG , CM000667.1:g.32748686_32748689delinsCTGG	GRCh37
NC_000005.8:g.32784443_32784446delinsCTGG	NCBI36
NG_028162.1:g.42944_42947delinsCTGG
NG_028162.2:g.64505_64508delinsCTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265074.13:c.1059+9550_1059+9553delinsCTGG MANE Select	ENSP00000265074.8:n.1059+9550_1059+9553delinsCTGG
ENST00000265074.12:c.1059+9550_1059+9553delinsCTGG	ENSP00000265074.8:n.1059+9550_1059+9553delinsCTGG
ENST00000326958.5:c.411+9550_411+9553delinsCTGG	ENSP00000318340.2:n.411+9550_411+9553delinsCTGG
ENST00000415167.2:c.1059+9550_1059+9553delinsCTGG	ENSP00000398028.2:n.1059+9550_1059+9553delinsCTGG
ENST00000434067.6:c.411+9550_411+9553delinsCTGG	ENSP00000388408.2:n.411+9550_411+9553delinsCTGG
ENST00000506712.1:n.420+9550_420+9553delinsCTGG
ENST00000509104.5:c.390+9550_390+9553delinsCTGG	ENSP00000425325.1:n.390+9550_390+9553delinsCTGG
NM_000908.3:c.1059+9550_1059+9553delinsCTGG	NP_000899.1:n.1059+9550_1059+9553delinsCTGG
NM_001204375.1:c.1059+9550_1059+9553delinsCTGG	NP_001191304.1:n.1059+9550_1059+9553delinsCTGG
NM_001204376.1:c.411+9550_411+9553delinsCTGG	NP_001191305.1:n.411+9550_411+9553delinsCTGG
XM_005248309.1:c.411+9550_411+9553delinsCTGG	XP_005248366.1:n.411+9550_411+9553delinsCTGG
XM_011514047.1:c.390+9550_390+9553delinsCTGG	XP_011512349.1:n.390+9550_390+9553delinsCTGG
XM_011514048.1:c.339+9550_339+9553delinsCTGG	XP_011512350.1:n.339+9550_339+9553delinsCTGG
XM_011514049.1:c.282+9550_282+9553delinsCTGG	XP_011512351.1:n.282+9550_282+9553delinsCTGG
NM_001363652.1:c.411+9550_411+9553delinsCTGG	NP_001350581.1:n.411+9550_411+9553delinsCTGG
NM_001364458.1:c.339+9550_339+9553delinsCTGG	NP_001351387.1:n.339+9550_339+9553delinsCTGG
NM_001364460.1:c.288+9550_288+9553delinsCTGG	NP_001351389.1:n.288+9550_288+9553delinsCTGG
XM_011514047.2:c.390+9550_390+9553delinsCTGG	XP_011512349.1:n.390+9550_390+9553delinsCTGG
XM_011514049.3:c.282+9550_282+9553delinsCTGG	XP_011512351.1:n.282+9550_282+9553delinsCTGG
XM_017009492.2:c.936+9550_936+9553delinsCTGG	XP_016864981.1:n.936+9550_936+9553delinsCTGG
NM_001204375.2:c.1059+9550_1059+9553delinsCTGG MANE Select	NP_001191304.1:n.1059+9550_1059+9553delinsCTGG
NM_000908.4:c.1059+9550_1059+9553delinsCTGG	NP_000899.1:n.1059+9550_1059+9553delinsCTGG
NM_001363652.2:c.411+9550_411+9553delinsCTGG	NP_001350581.1:n.411+9550_411+9553delinsCTGG
NM_001364458.2:c.339+9550_339+9553delinsCTGG	NP_001351387.1:n.339+9550_339+9553delinsCTGG
NM_001364460.2:c.288+9550_288+9553delinsCTGG	NP_001351389.1:n.288+9550_288+9553delinsCTGG
NM_001204376.2:c.411+9550_411+9553delinsCTGG	NP_001191305.1:n.411+9550_411+9553delinsCTGG