Canonical Allele Identifier: CA2480546016

Gene: NPR1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153683988_153683990delinsAAG , CM000663.2:g.153683988_153683990delinsAAG	GRCh38
NC_000001.10:g.153656464_153656466delinsAAG , CM000663.1:g.153656464_153656466delinsAAG	GRCh37
NC_000001.9:g.151923088_151923090delinsAAG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368680.4:c.1484+164_1484+166delinsAAG MANE Select	ENSP00000357669.3:n.1484+164_1484+166delinsAAG
ENST00000368680.3:c.1484+164_1484+166delinsAAG	ENSP00000357669.3:n.1484+164_1484+166delinsAAG
NM_000906.3:c.1484+164_1484+166delinsAAG	NP_000897.3:n.1484+164_1484+166delinsAAG
XM_005245218.1:c.1484+164_1484+166delinsAAG	XP_005245275.1:n.1484+164_1484+166delinsAAG
XM_006711342.1:c.1484+164_1484+166delinsAAG	XP_006711405.1:n.1484+164_1484+166delinsAAG
XM_006711343.1:c.1484+164_1484+166delinsAAG	XP_006711406.1:n.1484+164_1484+166delinsAAG
XM_011509585.1:c.1484+164_1484+166delinsAAG	XP_011507887.1:n.1484+164_1484+166delinsAAG
XM_005245218.2:c.1484+164_1484+166delinsAAG	XP_005245275.1:n.1484+164_1484+166delinsAAG
XM_017001374.2:c.1484+164_1484+166delinsAAG	XP_016856863.1:n.1484+164_1484+166delinsAAG
NM_000906.4:c.1484+164_1484+166delinsAAG MANE Select	NP_000897.3:n.1484+164_1484+166delinsAAG