Canonical Allele Identifier: CA2480545949

Gene: NPR1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153683838_153683839delinsTG , CM000663.2:g.153683838_153683839delinsTG	GRCh38
NC_000001.10:g.153656314_153656315delinsTG , CM000663.1:g.153656314_153656315delinsTG	GRCh37
NC_000001.9:g.151922938_151922939delinsTG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368680.4:c.1484+14_1484+15delinsTG MANE Select	ENSP00000357669.3:n.1484+14_1484+15delinsTG
ENST00000368680.3:c.1484+14_1484+15delinsTG	ENSP00000357669.3:n.1484+14_1484+15delinsTG
NM_000906.3:c.1484+14_1484+15delinsTG	NP_000897.3:n.1484+14_1484+15delinsTG
XM_005245218.1:c.1484+14_1484+15delinsTG	XP_005245275.1:n.1484+14_1484+15delinsTG
XM_006711342.1:c.1484+14_1484+15delinsTG	XP_006711405.1:n.1484+14_1484+15delinsTG
XM_006711343.1:c.1484+14_1484+15delinsTG	XP_006711406.1:n.1484+14_1484+15delinsTG
XM_011509585.1:c.1484+14_1484+15delinsTG	XP_011507887.1:n.1484+14_1484+15delinsTG
XM_005245218.2:c.1484+14_1484+15delinsTG	XP_005245275.1:n.1484+14_1484+15delinsTG
XM_017001374.2:c.1484+14_1484+15delinsTG	XP_016856863.1:n.1484+14_1484+15delinsTG
NM_000906.4:c.1484+14_1484+15delinsTG MANE Select	NP_000897.3:n.1484+14_1484+15delinsTG