Canonical Allele Identifier: CA30689389

Gene: NPR1

Linked Data

• dbSNP Id: rs764105312
• gnomAD v3: 1-153684141-C-T
• gnomAD v4: 1-153684141-C-T
• MyVariant Identifiers: chr1:g.153656617C>T (hg19) ; chr1:g.153684141C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153684141C>T , CM000663.2:g.153684141C>T	GRCh38
NC_000001.10:g.153656617C>T , CM000663.1:g.153656617C>T	GRCh37
NC_000001.9:g.151923241C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368680.4:c.1484+317C>T MANE Select	ENSP00000357669.3:n.1484+317C>T
ENST00000368680.3:c.1484+317C>T	ENSP00000357669.3:n.1484+317C>T
NM_000906.3:c.1484+317C>T	NP_000897.3:n.1484+317C>T
XM_005245218.1:c.1484+317C>T	XP_005245275.1:n.1484+317C>T
XM_006711342.1:c.1484+317C>T	XP_006711405.1:n.1484+317C>T
XM_006711343.1:c.1484+317C>T	XP_006711406.1:n.1484+317C>T
XM_011509585.1:c.1484+317C>T	XP_011507887.1:n.1484+317C>T
XM_005245218.2:c.1484+317C>T	XP_005245275.1:n.1484+317C>T
XM_017001374.2:c.1484+317C>T	XP_016856863.1:n.1484+317C>T
NM_000906.4:c.1484+317C>T MANE Select	NP_000897.3:n.1484+317C>T