Canonical Allele Identifier: CA526366216

Gene: NPR1

Linked Data

• dbSNP Id: rs1486759729
• gnomAD v2: 1-153656285-CCTT-C
• gnomAD v4: 1-153683809-CCTT-C
• MyVariant Identifiers: chr1:g.153656286_153656288del (hg19) ; chr1:g.153683810_153683812del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153683814_153683816del , CM000663.2:g.153683814_153683816del	GRCh38
NC_000001.10:g.153656290_153656292del , CM000663.1:g.153656290_153656292del	GRCh37
NC_000001.9:g.151922914_151922916del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368680.4:c.1474_1476del MANE Select	ENSP00000357669.3:p.Phe492del
ENST00000368680.3:c.1474_1476del	ENSP00000357669.3:p.Phe492del
NM_000906.3:c.1474_1476del	NP_000897.3:p.Phe492del
XM_005245218.1:c.1474_1476del	XP_005245275.1:p.Phe492del
XM_006711342.1:c.1474_1476del	XP_006711405.1:p.Phe492del
XM_006711343.1:c.1474_1476del	XP_006711406.1:p.Phe492del
XM_011509585.1:c.1474_1476del	XP_011507887.1:p.Phe492del
XM_005245218.2:c.1474_1476del	XP_005245275.1:p.Phe492del
XM_017001374.2:c.1474_1476del	XP_016856863.1:p.Phe492del
NM_000906.4:c.1474_1476del MANE Select	NP_000897.3:p.Phe492del