Canonical Allele Identifier: CA3165921349
Community Standard Title: NM_003995.4(NPR2):c.1758C= (p.Cys586=)
Gene: NPR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.35802550C= , CM000671.2:g.35802550C= GRCh38
NC_000009.11:g.35802547C= , CM000671.1:g.35802547C= GRCh37
NC_000009.10:g.35792547C= NCBI36
NG_009249.1:g.15142C=

Transcript Alleles

HGVS Amino-acid Change
NM_003995.4:c.1758C= MANE Select NP_003986.2:p.Cys586=
ENST00000342694.7:c.1758C= MANE Select ENSP00000341083.2:p.Cys586=
NM_001378923.1:c.1767C= NP_001365852.1:p.Cys589=
NM_003995.3:c.1758C= NP_003986.2:p.Cys586=
ENST00000342694.6:c.1758C= ENSP00000341083.2:p.Cys586=
ENST00000448821.6:c.1758C= ENSP00000402902.2:p.Cys586=
ENST00000464810.5:n.1758C=
ENST00000685871.1:c.1758C= ENSP00000509964.1:p.Cys586=
ENST00000686159.1:n.1797C=
ENST00000686486.1:n.928C=
ENST00000687302.1:n.1872C=
ENST00000687357.1:c.1683C= ENSP00000509549.1:p.Cys561=
ENST00000687625.1:n.913C=
ENST00000687787.1:c.1758C= ENSP00000509440.1:p.Cys586=
ENST00000688201.1:n.1715C=
ENST00000688226.1:n.1690C=
ENST00000688869.1:n.2064C=
ENST00000689788.1:c.1552C= ENSP00000508973.1:n.1552C=
ENST00000689898.1:c.1687C= ENSP00000509651.1:n.1687C=
ENST00000690070.1:c.1683C= ENSP00000509654.1:p.Cys561=
ENST00000690267.1:c.1547C= ENSP00000510432.1:n.1547C=
ENST00000690552.1:n.1619C=
ENST00000691138.1:n.1619C=
ENST00000691969.1:c.1258C= ENSP00000510244.1:n.1258C=
ENST00000692232.1:n.2914C=
ENST00000692233.1:c.1622C= ENSP00000509698.1:n.1622C=
ENST00000692380.1:n.913C=
ENST00000692447.1:n.2874C=
ENST00000693094.1:c.1758C= ENSP00000510161.1:p.Cys586=
XM_005251478.3:c.1767C= XP_005251535.1:p.Cys589=
XM_005251479.3:c.780C= XP_005251536.1:p.Cys260=
XM_006716778.2:c.1767C= XP_006716841.1:p.Cys589=
XM_011517889.1:c.780C= XP_011516191.1:p.Cys260=
XM_011517890.1:c.780C= XP_011516192.1:p.Cys260=
XM_011517891.1:c.780C= XP_011516193.1:p.Cys260=
XM_011517892.1:c.780C= XP_011516194.1:p.Cys260=
XM_011517893.1:c.780C= XP_011516195.1:p.Cys260=
XM_011517894.1:c.780C= XP_011516196.1:p.Cys260=
XM_011517895.1:c.363C= XP_011516197.1:p.Cys121=
XM_024447556.1:c.1767C= XP_024303324.1:p.Cys589=
XM_024447557.1:c.1758C= XP_024303325.1:p.Cys586=
XM_024447558.1:c.780C= XP_024303326.1:p.Cys260=
XM_024447559.1:c.363C= XP_024303327.1:p.Cys121=
XM_024447560.1:c.354C= XP_024303328.1:p.Cys118=
XM_024447561.1:c.354C= XP_024303329.1:p.Cys118=