Canonical Allele Identifier: CA2648068580

Gene: NPR1

Linked Data

• gnomAD v4: 1-153683959-A-ACTTTCT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153683959_153683960insCTTTCT , CM000663.2:g.153683959_153683960insCTTTCT	GRCh38
NC_000001.10:g.153656435_153656436insCTTTCT , CM000663.1:g.153656435_153656436insCTTTCT	GRCh37
NC_000001.9:g.151923059_151923060insCTTTCT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368680.4:c.1484+135_1484+136insCTTTCT MANE Select	ENSP00000357669.3:n.1484+135_1484+136insCTTTCT
ENST00000368680.3:c.1484+135_1484+136insCTTTCT	ENSP00000357669.3:n.1484+135_1484+136insCTTTCT
NM_000906.3:c.1484+135_1484+136insCTTTCT	NP_000897.3:n.1484+135_1484+136insCTTTCT
XM_005245218.1:c.1484+135_1484+136insCTTTCT	XP_005245275.1:n.1484+135_1484+136insCTTTCT
XM_006711342.1:c.1484+135_1484+136insCTTTCT	XP_006711405.1:n.1484+135_1484+136insCTTTCT
XM_006711343.1:c.1484+135_1484+136insCTTTCT	XP_006711406.1:n.1484+135_1484+136insCTTTCT
XM_011509585.1:c.1484+135_1484+136insCTTTCT	XP_011507887.1:n.1484+135_1484+136insCTTTCT
XM_005245218.2:c.1484+135_1484+136insCTTTCT	XP_005245275.1:n.1484+135_1484+136insCTTTCT
XM_017001374.2:c.1484+135_1484+136insCTTTCT	XP_016856863.1:n.1484+135_1484+136insCTTTCT
NM_000906.4:c.1484+135_1484+136insCTTTCT MANE Select	NP_000897.3:n.1484+135_1484+136insCTTTCT