Canonical Allele Identifier: CA342521966

Gene: NPR1

Linked Data

• gnomAD v4: 1-153683766-G-T
• MyVariant Identifiers: chr1:g.153656242G>T (hg19) ; chr1:g.153683766G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153683766G>T , CM000663.2:g.153683766G>T	GRCh38
NC_000001.10:g.153656242G>T , CM000663.1:g.153656242G>T	GRCh37
NC_000001.9:g.151922866G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368680.4:c.1426G>T MANE Select	ENSP00000357669.3:p.Ala476Ser
ENST00000368680.3:c.1426G>T	ENSP00000357669.3:p.Ala476Ser
NM_000906.3:c.1426G>T	NP_000897.3:p.Ala476Ser
XM_005245218.1:c.1426G>T	XP_005245275.1:p.Ala476Ser
XM_006711342.1:c.1426G>T	XP_006711405.1:p.Ala476Ser
XM_006711343.1:c.1426G>T	XP_006711406.1:p.Ala476Ser
XM_011509585.1:c.1426G>T	XP_011507887.1:p.Ala476Ser
XM_005245218.2:c.1426G>T	XP_005245275.1:p.Ala476Ser
XM_017001374.2:c.1426G>T	XP_016856863.1:p.Ala476Ser
NM_000906.4:c.1426G>T MANE Select	NP_000897.3:p.Ala476Ser