Canonical Allele Identifier: CA342521969
Gene: NPR1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.153683767C>T , CM000663.2:g.153683767C>T GRCh38
NC_000001.10:g.153656243C>T , CM000663.1:g.153656243C>T GRCh37
NC_000001.9:g.151922867C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368680.4:c.1427C>T MANE Select ENSP00000357669.3:p.Ala476Val
ENST00000368680.3:c.1427C>T ENSP00000357669.3:p.Ala476Val
NM_000906.3:c.1427C>T NP_000897.3:p.Ala476Val
XM_005245218.1:c.1427C>T XP_005245275.1:p.Ala476Val
XM_006711342.1:c.1427C>T XP_006711405.1:p.Ala476Val
XM_006711343.1:c.1427C>T XP_006711406.1:p.Ala476Val
XM_011509585.1:c.1427C>T XP_011507887.1:p.Ala476Val
XM_005245218.2:c.1427C>T XP_005245275.1:p.Ala476Val
XM_017001374.2:c.1427C>T XP_016856863.1:p.Ala476Val
NM_000906.4:c.1427C>T MANE Select NP_000897.3:p.Ala476Val