Canonical Allele Identifier: CA30689320

Gene: NPR1

Linked Data

• dbSNP Id: rs144094762
• gnomAD v2: 1-153656564-T-C
• gnomAD v3: 1-153684088-T-C
• gnomAD v4: 1-153684088-T-C
• MyVariant Identifiers: chr1:g.153656564T>C (hg19) ; chr1:g.153684088T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153684088T>C , CM000663.2:g.153684088T>C	GRCh38
NC_000001.10:g.153656564T>C , CM000663.1:g.153656564T>C	GRCh37
NC_000001.9:g.151923188T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368680.4:c.1484+264T>C MANE Select	ENSP00000357669.3:n.1484+264T>C
ENST00000368680.3:c.1484+264T>C	ENSP00000357669.3:n.1484+264T>C
NM_000906.3:c.1484+264T>C	NP_000897.3:n.1484+264T>C
XM_005245218.1:c.1484+264T>C	XP_005245275.1:n.1484+264T>C
XM_006711342.1:c.1484+264T>C	XP_006711405.1:n.1484+264T>C
XM_006711343.1:c.1484+264T>C	XP_006711406.1:n.1484+264T>C
XM_011509585.1:c.1484+264T>C	XP_011507887.1:n.1484+264T>C
XM_005245218.2:c.1484+264T>C	XP_005245275.1:n.1484+264T>C
XM_017001374.2:c.1484+264T>C	XP_016856863.1:n.1484+264T>C
NM_000906.4:c.1484+264T>C MANE Select	NP_000897.3:n.1484+264T>C