Canonical Allele Identifier: CA1118079
Gene: NPR1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3201748
ClinVar RCV Id: RCV004491093
dbSNP Id: rs766597678
ExAC: 1:153656233 G / A
gnomAD v2: 1-153656233-G-A
gnomAD v3: 1-153683757-G-A
gnomAD v4: 1-153683757-G-A
MyVariant Identifiers: chr1:g.153656233G>A (hg19) chr1:g.153683757G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.153683757G>A , CM000663.2:g.153683757G>A GRCh38
NC_000001.10:g.153656233G>A , CM000663.1:g.153656233G>A GRCh37
NC_000001.9:g.151922857G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368680.4:c.1417G>A MANE Select ENSP00000357669.3:p.Glu473Lys
ENST00000368680.3:c.1417G>A ENSP00000357669.3:p.Glu473Lys
NM_000906.3:c.1417G>A NP_000897.3:p.Glu473Lys
XM_005245218.1:c.1417G>A XP_005245275.1:p.Glu473Lys
XM_006711342.1:c.1417G>A XP_006711405.1:p.Glu473Lys
XM_006711343.1:c.1417G>A XP_006711406.1:p.Glu473Lys
XM_011509585.1:c.1417G>A XP_011507887.1:p.Glu473Lys
XM_005245218.2:c.1417G>A XP_005245275.1:p.Glu473Lys
XM_017001374.2:c.1417G>A XP_016856863.1:p.Glu473Lys
NM_000906.4:c.1417G>A MANE Select NP_000897.3:p.Glu473Lys
Search 100 bp 5'
Search 100 bp 3'