Canonical Allele Identifier: CA2480546099

Gene: NPR1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153684213C= , CM000663.2:g.153684213C=	GRCh38
NC_000001.10:g.153656689C= , CM000663.1:g.153656689C=	GRCh37
NC_000001.9:g.151923313C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368680.4:c.1484+389C= MANE Select	ENSP00000357669.3:n.1484+389C=
ENST00000368680.3:c.1484+389C=	ENSP00000357669.3:n.1484+389C=
NM_000906.3:c.1484+389C=	NP_000897.3:n.1484+389C=
XM_005245218.1:c.1484+389C=	XP_005245275.1:n.1484+389C=
XM_006711342.1:c.1484+389C=	XP_006711405.1:n.1484+389C=
XM_006711343.1:c.1484+389C=	XP_006711406.1:n.1484+389C=
XM_011509585.1:c.1484+389C=	XP_011507887.1:n.1484+389C=
XM_005245218.2:c.1484+389C=	XP_005245275.1:n.1484+389C=
XM_017001374.2:c.1484+389C=	XP_016856863.1:n.1484+389C=
NM_000906.4:c.1484+389C= MANE Select	NP_000897.3:n.1484+389C=