Canonical Allele Identifier: CA2480546100

Gene: NPR1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153684215A= , CM000663.2:g.153684215A=	GRCh38
NC_000001.10:g.153656691A= , CM000663.1:g.153656691A=	GRCh37
NC_000001.9:g.151923315A=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000368680.4:c.1484+391A= MANE Select	ENSP00000357669.3:n.1484+391A=
ENST00000368680.3:c.1484+391A=	ENSP00000357669.3:n.1484+391A=
NM_000906.3:c.1484+391A=	NP_000897.3:n.1484+391A=
XM_005245218.1:c.1484+391A=	XP_005245275.1:n.1484+391A=
XM_006711342.1:c.1484+391A=	XP_006711405.1:n.1484+391A=
XM_006711343.1:c.1484+391A=	XP_006711406.1:n.1484+391A=
XM_011509585.1:c.1484+391A=	XP_011507887.1:n.1484+391A=
XM_005245218.2:c.1484+391A=	XP_005245275.1:n.1484+391A=
XM_017001374.2:c.1484+391A=	XP_016856863.1:n.1484+391A=
NM_000906.4:c.1484+391A= MANE Select	NP_000897.3:n.1484+391A=