Canonical Allele Identifier: CA2480546047
Gene: NPR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.153684063G= , CM000663.2:g.153684063G= GRCh38
NC_000001.10:g.153656539G= , CM000663.1:g.153656539G= GRCh37
NC_000001.9:g.151923163G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368680.4:c.1484+239G= MANE Select ENSP00000357669.3:n.1484+239G=
ENST00000368680.3:c.1484+239G= ENSP00000357669.3:n.1484+239G=
NM_000906.3:c.1484+239G= NP_000897.3:n.1484+239G=
XM_005245218.1:c.1484+239G= XP_005245275.1:n.1484+239G=
XM_006711342.1:c.1484+239G= XP_006711405.1:n.1484+239G=
XM_006711343.1:c.1484+239G= XP_006711406.1:n.1484+239G=
XM_011509585.1:c.1484+239G= XP_011507887.1:n.1484+239G=
XM_005245218.2:c.1484+239G= XP_005245275.1:n.1484+239G=
XM_017001374.2:c.1484+239G= XP_016856863.1:n.1484+239G=
NM_000906.4:c.1484+239G= MANE Select NP_000897.3:n.1484+239G=