Canonical Allele Identifier: CA1148722894

Gene: NPR1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153683839_153683844delinsGGGGGG , CM000663.2:g.153683839_153683844delinsGGGGGG	GRCh38
NC_000001.10:g.153656315_153656320delinsGGGGGG , CM000663.1:g.153656315_153656320delinsGGGGGG	GRCh37
NC_000001.9:g.151922939_151922944delinsGGGGGG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368680.4:c.1484+15_1484+20delinsGGGGGG MANE Select	ENSP00000357669.3:n.1484+15_1484+20delinsGGGGGG
ENST00000368680.3:c.1484+15_1484+20delinsGGGGGG	ENSP00000357669.3:n.1484+15_1484+20delinsGGGGGG
NM_000906.3:c.1484+15_1484+20delinsGGGGGG	NP_000897.3:n.1484+15_1484+20delinsGGGGGG
XM_005245218.1:c.1484+15_1484+20delinsGGGGGG	XP_005245275.1:n.1484+15_1484+20delinsGGGGGG
XM_006711342.1:c.1484+15_1484+20delinsGGGGGG	XP_006711405.1:n.1484+15_1484+20delinsGGGGGG
XM_006711343.1:c.1484+15_1484+20delinsGGGGGG	XP_006711406.1:n.1484+15_1484+20delinsGGGGGG
XM_011509585.1:c.1484+15_1484+20delinsGGGGGG	XP_011507887.1:n.1484+15_1484+20delinsGGGGGG
XM_005245218.2:c.1484+15_1484+20delinsGGGGGG	XP_005245275.1:n.1484+15_1484+20delinsGGGGGG
XM_017001374.2:c.1484+15_1484+20delinsGGGGGG	XP_016856863.1:n.1484+15_1484+20delinsGGGGGG
NM_000906.4:c.1484+15_1484+20delinsGGGGGG MANE Select	NP_000897.3:n.1484+15_1484+20delinsGGGGGG