Canonical Allele Identifier: CA2648068308

Gene: NPR1

Linked Data

• gnomAD v4: 1-153683857-GGGGGACCCGGAGAACCAATAGCAGAGGAGGCGGT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153683866_153683899del , CM000663.2:g.153683866_153683899del	GRCh38
NC_000001.10:g.153656342_153656375del , CM000663.1:g.153656342_153656375del	GRCh37
NC_000001.9:g.151922966_151922999del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368680.4:c.1484+42_1484+75del MANE Select	ENSP00000357669.3:n.1484+42_1484+75del
ENST00000368680.3:c.1484+42_1484+75del	ENSP00000357669.3:n.1484+42_1484+75del
NM_000906.3:c.1484+42_1484+75del	NP_000897.3:n.1484+42_1484+75del
XM_005245218.1:c.1484+42_1484+75del	XP_005245275.1:n.1484+42_1484+75del
XM_006711342.1:c.1484+42_1484+75del	XP_006711405.1:n.1484+42_1484+75del
XM_006711343.1:c.1484+42_1484+75del	XP_006711406.1:n.1484+42_1484+75del
XM_011509585.1:c.1484+42_1484+75del	XP_011507887.1:n.1484+42_1484+75del
XM_005245218.2:c.1484+42_1484+75del	XP_005245275.1:n.1484+42_1484+75del
XM_017001374.2:c.1484+42_1484+75del	XP_016856863.1:n.1484+42_1484+75del
NM_000906.4:c.1484+42_1484+75del MANE Select	NP_000897.3:n.1484+42_1484+75del