Canonical Allele Identifier: CA2480545932

Gene: NPR1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153683803T= , CM000663.2:g.153683803T=	GRCh38
NC_000001.10:g.153656279T= , CM000663.1:g.153656279T=	GRCh37
NC_000001.9:g.151922903T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368680.4:c.1463T= MANE Select	ENSP00000357669.3:p.Ile488=
ENST00000368680.3:c.1463T=	ENSP00000357669.3:p.Ile488=
NM_000906.3:c.1463T=	NP_000897.3:p.Ile488=
XM_005245218.1:c.1463T=	XP_005245275.1:p.Ile488=
XM_006711342.1:c.1463T=	XP_006711405.1:p.Ile488=
XM_006711343.1:c.1463T=	XP_006711406.1:p.Ile488=
XM_011509585.1:c.1463T=	XP_011507887.1:p.Ile488=
XM_005245218.2:c.1463T=	XP_005245275.1:p.Ile488=
XM_017001374.2:c.1463T=	XP_016856863.1:p.Ile488=
NM_000906.4:c.1463T= MANE Select	NP_000897.3:p.Ile488=