Canonical Allele Identifier: CA2648068588

Gene: NPR1

Linked Data

• gnomAD v4: 1-153683963-A-AGG

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153683964_153683965dup , CM000663.2:g.153683964_153683965dup	GRCh38
NC_000001.10:g.153656440_153656441dup , CM000663.1:g.153656440_153656441dup	GRCh37
NC_000001.9:g.151923064_151923065dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368680.4:c.1484+140_1484+141dup MANE Select	ENSP00000357669.3:n.1484+140_1484+141dup
ENST00000368680.3:c.1484+140_1484+141dup	ENSP00000357669.3:n.1484+140_1484+141dup
NM_000906.3:c.1484+140_1484+141dup	NP_000897.3:n.1484+140_1484+141dup
XM_005245218.1:c.1484+140_1484+141dup	XP_005245275.1:n.1484+140_1484+141dup
XM_006711342.1:c.1484+140_1484+141dup	XP_006711405.1:n.1484+140_1484+141dup
XM_006711343.1:c.1484+140_1484+141dup	XP_006711406.1:n.1484+140_1484+141dup
XM_011509585.1:c.1484+140_1484+141dup	XP_011507887.1:n.1484+140_1484+141dup
XM_005245218.2:c.1484+140_1484+141dup	XP_005245275.1:n.1484+140_1484+141dup
XM_017001374.2:c.1484+140_1484+141dup	XP_016856863.1:n.1484+140_1484+141dup
NM_000906.4:c.1484+140_1484+141dup MANE Select	NP_000897.3:n.1484+140_1484+141dup