Canonical Allele Identifier: CA342521900

Gene: NPR1

Linked Data

• ClinVar Variation Id: 2547188
• ClinVar RCV Id: RCV004321246
• gnomAD v4: 1-153683741-T-A
• MyVariant Identifiers: chr1:g.153656217T>A (hg19) ; chr1:g.153683741T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153683741T>A , CM000663.2:g.153683741T>A	GRCh38
NC_000001.10:g.153656217T>A , CM000663.1:g.153656217T>A	GRCh37
NC_000001.9:g.151922841T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368680.4:c.1401T>A MANE Select	ENSP00000357669.3:p.Asp467Glu
ENST00000368680.3:c.1401T>A	ENSP00000357669.3:p.Asp467Glu
NM_000906.3:c.1401T>A	NP_000897.3:p.Asp467Glu
XM_005245218.1:c.1401T>A	XP_005245275.1:p.Asp467Glu
XM_006711342.1:c.1401T>A	XP_006711405.1:p.Asp467Glu
XM_006711343.1:c.1401T>A	XP_006711406.1:p.Asp467Glu
XM_011509585.1:c.1401T>A	XP_011507887.1:p.Asp467Glu
XM_005245218.2:c.1401T>A	XP_005245275.1:p.Asp467Glu
XM_017001374.2:c.1401T>A	XP_016856863.1:p.Asp467Glu
NM_000906.4:c.1401T>A MANE Select	NP_000897.3:p.Asp467Glu