Canonical Allele Identifier: CA2480546057
Gene: NPR1 HGNC NCBI

Linked Data

dbSNP Id: rs1669860682
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.153684087A>C , CM000663.2:g.153684087A>C GRCh38
NC_000001.10:g.153656563A>C , CM000663.1:g.153656563A>C GRCh37
NC_000001.9:g.151923187A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000368680.4:c.1484+263A>C MANE Select ENSP00000357669.3:n.1484+263A>C
ENST00000368680.3:c.1484+263A>C ENSP00000357669.3:n.1484+263A>C
NM_000906.3:c.1484+263A>C NP_000897.3:n.1484+263A>C
XM_005245218.1:c.1484+263A>C XP_005245275.1:n.1484+263A>C
XM_006711342.1:c.1484+263A>C XP_006711405.1:n.1484+263A>C
XM_006711343.1:c.1484+263A>C XP_006711406.1:n.1484+263A>C
XM_011509585.1:c.1484+263A>C XP_011507887.1:n.1484+263A>C
XM_005245218.2:c.1484+263A>C XP_005245275.1:n.1484+263A>C
XM_017001374.2:c.1484+263A>C XP_016856863.1:n.1484+263A>C
NM_000906.4:c.1484+263A>C MANE Select NP_000897.3:n.1484+263A>C
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