Canonical Allele Identifier: CA889511487

Gene: NPR1

Linked Data

• dbSNP Id: rs1180585480
• gnomAD v3: 1-153683988-AAG-A
• gnomAD v4: 1-153683988-AAG-A
• MyVariant Identifiers: chr1:g.153656465_153656466del (hg19) ; chr1:g.153683989_153683990del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153683992_153683993del , CM000663.2:g.153683992_153683993del	GRCh38
NC_000001.10:g.153656468_153656469del , CM000663.1:g.153656468_153656469del	GRCh37
NC_000001.9:g.151923092_151923093del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368680.4:c.1484+168_1484+169del MANE Select	ENSP00000357669.3:n.1484+168_1484+169del
ENST00000368680.3:c.1484+168_1484+169del	ENSP00000357669.3:n.1484+168_1484+169del
NM_000906.3:c.1484+168_1484+169del	NP_000897.3:n.1484+168_1484+169del
XM_005245218.1:c.1484+168_1484+169del	XP_005245275.1:n.1484+168_1484+169del
XM_006711342.1:c.1484+168_1484+169del	XP_006711405.1:n.1484+168_1484+169del
XM_006711343.1:c.1484+168_1484+169del	XP_006711406.1:n.1484+168_1484+169del
XM_011509585.1:c.1484+168_1484+169del	XP_011507887.1:n.1484+168_1484+169del
XM_005245218.2:c.1484+168_1484+169del	XP_005245275.1:n.1484+168_1484+169del
XM_017001374.2:c.1484+168_1484+169del	XP_016856863.1:n.1484+168_1484+169del
NM_000906.4:c.1484+168_1484+169del MANE Select	NP_000897.3:n.1484+168_1484+169del