Canonical Allele Identifier: CA1007858914

Gene: NPR1

Linked Data

• gnomAD v3: 1-153683941-CAAGGGAGATGAGGAAGA-C
• gnomAD v4: 1-153683941-CAAGGGAGATGAGGAAGA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153683946_153683962del , CM000663.2:g.153683946_153683962del	GRCh38
NC_000001.10:g.153656422_153656438del , CM000663.1:g.153656422_153656438del	GRCh37
NC_000001.9:g.151923046_151923062del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368680.4:c.1484+122_1484+138del MANE Select	ENSP00000357669.3:n.1484+122_1484+138del
ENST00000368680.3:c.1484+122_1484+138del	ENSP00000357669.3:n.1484+122_1484+138del
NM_000906.3:c.1484+122_1484+138del	NP_000897.3:n.1484+122_1484+138del
XM_005245218.1:c.1484+122_1484+138del	XP_005245275.1:n.1484+122_1484+138del
XM_006711342.1:c.1484+122_1484+138del	XP_006711405.1:n.1484+122_1484+138del
XM_006711343.1:c.1484+122_1484+138del	XP_006711406.1:n.1484+122_1484+138del
XM_011509585.1:c.1484+122_1484+138del	XP_011507887.1:n.1484+122_1484+138del
XM_005245218.2:c.1484+122_1484+138del	XP_005245275.1:n.1484+122_1484+138del
XM_017001374.2:c.1484+122_1484+138del	XP_016856863.1:n.1484+122_1484+138del
NM_000906.4:c.1484+122_1484+138del MANE Select	NP_000897.3:n.1484+122_1484+138del