Canonical Allele Identifier: CA889511442

Gene: NPR1

Linked Data

• dbSNP Id: rs1376632859
• gnomAD v3: 1-153683925-GGC-G
• gnomAD v4: 1-153683925-GGC-G
• MyVariant Identifiers: chr1:g.153656402_153656403del (hg19) ; chr1:g.153683926_153683927del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153683926_153683927del , CM000663.2:g.153683926_153683927del	GRCh38
NC_000001.10:g.153656402_153656403del , CM000663.1:g.153656402_153656403del	GRCh37
NC_000001.9:g.151923026_151923027del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368680.4:c.1484+102_1484+103del MANE Select	ENSP00000357669.3:n.1484+102_1484+103del
ENST00000368680.3:c.1484+102_1484+103del	ENSP00000357669.3:n.1484+102_1484+103del
NM_000906.3:c.1484+102_1484+103del	NP_000897.3:n.1484+102_1484+103del
XM_005245218.1:c.1484+102_1484+103del	XP_005245275.1:n.1484+102_1484+103del
XM_006711342.1:c.1484+102_1484+103del	XP_006711405.1:n.1484+102_1484+103del
XM_006711343.1:c.1484+102_1484+103del	XP_006711406.1:n.1484+102_1484+103del
XM_011509585.1:c.1484+102_1484+103del	XP_011507887.1:n.1484+102_1484+103del
XM_005245218.2:c.1484+102_1484+103del	XP_005245275.1:n.1484+102_1484+103del
XM_017001374.2:c.1484+102_1484+103del	XP_016856863.1:n.1484+102_1484+103del
NM_000906.4:c.1484+102_1484+103del MANE Select	NP_000897.3:n.1484+102_1484+103del