Canonical Allele Identifier: CA2480546118
Gene: NPR1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.153684265C= , CM000663.2:g.153684265C= GRCh38
NC_000001.10:g.153656741C= , CM000663.1:g.153656741C= GRCh37
NC_000001.9:g.151923365C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368680.4:c.1484+441C= MANE Select ENSP00000357669.3:n.1484+441C=
ENST00000368680.3:c.1484+441C= ENSP00000357669.3:n.1484+441C=
NM_000906.3:c.1484+441C= NP_000897.3:n.1484+441C=
XM_005245218.1:c.1484+441C= XP_005245275.1:n.1484+441C=
XM_006711342.1:c.1484+441C= XP_006711405.1:n.1484+441C=
XM_006711343.1:c.1484+441C= XP_006711406.1:n.1484+441C=
XM_011509585.1:c.1484+441C= XP_011507887.1:n.1484+441C=
XM_005245218.2:c.1484+441C= XP_005245275.1:n.1484+441C=
XM_017001374.2:c.1484+441C= XP_016856863.1:n.1484+441C=
NM_000906.4:c.1484+441C= MANE Select NP_000897.3:n.1484+441C=
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