Canonical Allele Identifier: CA1846133607
Gene: NPR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.35801130G= , CM000671.2:g.35801130G= GRCh38
NC_000009.11:g.35801127G= , CM000671.1:g.35801127G= GRCh37
NC_000009.10:g.35791127G= NCBI36
NG_009249.1:g.13722G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000448821.6:c.1412G= ENSP00000402902.2:p.Gly471=
ENST00000685871.1:c.1412G= ENSP00000509964.1:p.Gly471=
ENST00000686159.1:n.1451G=
ENST00000686486.1:n.420G=
ENST00000687302.1:n.1498G=
ENST00000687357.1:c.1412G= ENSP00000509549.1:p.Gly471=
ENST00000687625.1:n.567G=
ENST00000687787.1:c.1412G= ENSP00000509440.1:p.Gly471=
ENST00000688201.1:n.1444G=
ENST00000688226.1:n.1344G=
ENST00000688869.1:n.1718G=
ENST00000689788.1:c.1206G= ENSP00000508973.1:n.1206G=
ENST00000689898.1:c.1416G= ENSP00000509651.1:p.Trp472=
ENST00000690070.1:c.1412G= ENSP00000509654.1:p.Gly471=
ENST00000690267.1:c.1276G= ENSP00000510432.1:n.1276G=
ENST00000690552.1:n.1273G=
ENST00000691138.1:n.1273G=
ENST00000691969.1:c.987G= ENSP00000510244.1:n.987G=
ENST00000692232.1:n.2568G=
ENST00000692233.1:c.1276G= ENSP00000509698.1:n.1276G=
ENST00000692380.1:n.567G=
ENST00000692447.1:n.2528G=
ENST00000693094.1:c.1412G= ENSP00000510161.1:p.Gly471=
ENST00000342694.7:c.1412G= MANE Select ENSP00000341083.2:p.Gly471=
ENST00000342694.6:c.1412G= ENSP00000341083.2:p.Gly471=
ENST00000464810.5:n.1412G=
NM_003995.3:c.1412G= NP_003986.2:p.Gly471=
XM_005251478.3:c.1412G= XP_005251535.1:p.Gly471=
XM_005251479.3:c.425G= XP_005251536.1:p.Gly142=
XM_006716778.2:c.1412G= XP_006716841.1:p.Gly471=
XM_011517889.1:c.425G= XP_011516191.1:p.Gly142=
XM_011517890.1:c.425G= XP_011516192.1:p.Gly142=
XM_011517891.1:c.425G= XP_011516193.1:p.Gly142=
XM_011517892.1:c.425G= XP_011516194.1:p.Gly142=
XM_011517893.1:c.425G= XP_011516195.1:p.Gly142=
XM_011517894.1:c.425G= XP_011516196.1:p.Gly142=
XM_011517895.1:c.8G= XP_011516197.1:p.Gly3=
XM_024447556.1:c.1412G= XP_024303324.1:p.Gly471=
XM_024447557.1:c.1412G= XP_024303325.1:p.Gly471=
XM_024447558.1:c.425G= XP_024303326.1:p.Gly142=
XM_024447559.1:c.8G= XP_024303327.1:p.Gly3=
XM_024447560.1:c.8G= XP_024303328.1:p.Gly3=
XM_024447561.1:c.8G= XP_024303329.1:p.Gly3=
NM_003995.4:c.1412G= MANE Select NP_003986.2:p.Gly471=
NM_001378923.1:c.1412G= NP_001365852.1:p.Gly471=