Canonical Allele Identifier: CA2604792969

Gene: NPR1

Linked Data

• dbSNP Id: rs2101732111
• gnomAD v3: 1-153684044-A-ATCCAAGGAATG
• gnomAD v4: 1-153684044-A-ATCCAAGGAATG

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153684044_153684045insTCCAAGGAATG , CM000663.2:g.153684044_153684045insTCCAAGGAATG	GRCh38
NC_000001.10:g.153656520_153656521insTCCAAGGAATG , CM000663.1:g.153656520_153656521insTCCAAGGAATG	GRCh37
NC_000001.9:g.151923144_151923145insTCCAAGGAATG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368680.4:c.1484+220_1484+221insTCCAAGGAATG MANE Select	ENSP00000357669.3:n.1484+220_1484+221insTCCAAGGAATG
ENST00000368680.3:c.1484+220_1484+221insTCCAAGGAATG	ENSP00000357669.3:n.1484+220_1484+221insTCCAAGGAATG
NM_000906.3:c.1484+220_1484+221insTCCAAGGAATG	NP_000897.3:n.1484+220_1484+221insTCCAAGGAATG
XM_005245218.1:c.1484+220_1484+221insTCCAAGGAATG	XP_005245275.1:n.1484+220_1484+221insTCCAAGGAATG
XM_006711342.1:c.1484+220_1484+221insTCCAAGGAATG	XP_006711405.1:n.1484+220_1484+221insTCCAAGGAATG
XM_006711343.1:c.1484+220_1484+221insTCCAAGGAATG	XP_006711406.1:n.1484+220_1484+221insTCCAAGGAATG
XM_011509585.1:c.1484+220_1484+221insTCCAAGGAATG	XP_011507887.1:n.1484+220_1484+221insTCCAAGGAATG
XM_005245218.2:c.1484+220_1484+221insTCCAAGGAATG	XP_005245275.1:n.1484+220_1484+221insTCCAAGGAATG
XM_017001374.2:c.1484+220_1484+221insTCCAAGGAATG	XP_016856863.1:n.1484+220_1484+221insTCCAAGGAATG
NM_000906.4:c.1484+220_1484+221insTCCAAGGAATG MANE Select	NP_000897.3:n.1484+220_1484+221insTCCAAGGAATG