Canonical Allele Identifier: CA2480546067

Gene: NPR1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153684115_153684117delinsACT , CM000663.2:g.153684115_153684117delinsACT	GRCh38
NC_000001.10:g.153656591_153656593delinsACT , CM000663.1:g.153656591_153656593delinsACT	GRCh37
NC_000001.9:g.151923215_151923217delinsACT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368680.4:c.1484+291_1484+293delinsACT MANE Select	ENSP00000357669.3:n.1484+291_1484+293delinsACT
ENST00000368680.3:c.1484+291_1484+293delinsACT	ENSP00000357669.3:n.1484+291_1484+293delinsACT
NM_000906.3:c.1484+291_1484+293delinsACT	NP_000897.3:n.1484+291_1484+293delinsACT
XM_005245218.1:c.1484+291_1484+293delinsACT	XP_005245275.1:n.1484+291_1484+293delinsACT
XM_006711342.1:c.1484+291_1484+293delinsACT	XP_006711405.1:n.1484+291_1484+293delinsACT
XM_006711343.1:c.1484+291_1484+293delinsACT	XP_006711406.1:n.1484+291_1484+293delinsACT
XM_011509585.1:c.1484+291_1484+293delinsACT	XP_011507887.1:n.1484+291_1484+293delinsACT
XM_005245218.2:c.1484+291_1484+293delinsACT	XP_005245275.1:n.1484+291_1484+293delinsACT
XM_017001374.2:c.1484+291_1484+293delinsACT	XP_016856863.1:n.1484+291_1484+293delinsACT
NM_000906.4:c.1484+291_1484+293delinsACT MANE Select	NP_000897.3:n.1484+291_1484+293delinsACT