Canonical Allele Identifier: CA1537659415

Gene: NPR3

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.32748790_32748792delinsAAT , CM000667.2:g.32748790_32748792delinsAAT	GRCh38
NC_000005.9:g.32748896_32748898delinsAAT , CM000667.1:g.32748896_32748898delinsAAT	GRCh37
NC_000005.8:g.32784653_32784655delinsAAT	NCBI36
NG_028162.1:g.43154_43156delinsAAT
NG_028162.2:g.64715_64717delinsAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265074.13:c.1059+9760_1059+9762delinsAAT MANE Select	ENSP00000265074.8:n.1059+9760_1059+9762delinsAAT
ENST00000265074.12:c.1059+9760_1059+9762delinsAAT	ENSP00000265074.8:n.1059+9760_1059+9762delinsAAT
ENST00000326958.5:c.411+9760_411+9762delinsAAT	ENSP00000318340.2:n.411+9760_411+9762delinsAAT
ENST00000415167.2:c.1059+9760_1059+9762delinsAAT	ENSP00000398028.2:n.1059+9760_1059+9762delinsAAT
ENST00000434067.6:c.411+9760_411+9762delinsAAT	ENSP00000388408.2:n.411+9760_411+9762delinsAAT
ENST00000506712.1:n.420+9760_420+9762delinsAAT
ENST00000509104.5:c.390+9760_390+9762delinsAAT	ENSP00000425325.1:n.390+9760_390+9762delinsAAT
NM_000908.3:c.1059+9760_1059+9762delinsAAT	NP_000899.1:n.1059+9760_1059+9762delinsAAT
NM_001204375.1:c.1059+9760_1059+9762delinsAAT	NP_001191304.1:n.1059+9760_1059+9762delinsAAT
NM_001204376.1:c.411+9760_411+9762delinsAAT	NP_001191305.1:n.411+9760_411+9762delinsAAT
XM_005248309.1:c.411+9760_411+9762delinsAAT	XP_005248366.1:n.411+9760_411+9762delinsAAT
XM_011514047.1:c.390+9760_390+9762delinsAAT	XP_011512349.1:n.390+9760_390+9762delinsAAT
XM_011514048.1:c.339+9760_339+9762delinsAAT	XP_011512350.1:n.339+9760_339+9762delinsAAT
XM_011514049.1:c.282+9760_282+9762delinsAAT	XP_011512351.1:n.282+9760_282+9762delinsAAT
NM_001363652.1:c.411+9760_411+9762delinsAAT	NP_001350581.1:n.411+9760_411+9762delinsAAT
NM_001364458.1:c.339+9760_339+9762delinsAAT	NP_001351387.1:n.339+9760_339+9762delinsAAT
NM_001364460.1:c.288+9760_288+9762delinsAAT	NP_001351389.1:n.288+9760_288+9762delinsAAT
XM_011514047.2:c.390+9760_390+9762delinsAAT	XP_011512349.1:n.390+9760_390+9762delinsAAT
XM_011514049.3:c.282+9760_282+9762delinsAAT	XP_011512351.1:n.282+9760_282+9762delinsAAT
XM_017009492.2:c.936+9760_936+9762delinsAAT	XP_016864981.1:n.936+9760_936+9762delinsAAT
NM_001204375.2:c.1059+9760_1059+9762delinsAAT MANE Select	NP_001191304.1:n.1059+9760_1059+9762delinsAAT
NM_000908.4:c.1059+9760_1059+9762delinsAAT	NP_000899.1:n.1059+9760_1059+9762delinsAAT
NM_001363652.2:c.411+9760_411+9762delinsAAT	NP_001350581.1:n.411+9760_411+9762delinsAAT
NM_001364458.2:c.339+9760_339+9762delinsAAT	NP_001351387.1:n.339+9760_339+9762delinsAAT
NM_001364460.2:c.288+9760_288+9762delinsAAT	NP_001351389.1:n.288+9760_288+9762delinsAAT
NM_001204376.2:c.411+9760_411+9762delinsAAT	NP_001191305.1:n.411+9760_411+9762delinsAAT