Canonical Allele Identifier: CA1846132426
Gene: NPR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.35800729A= , CM000671.2:g.35800729A= GRCh38
NC_000009.11:g.35800726A= , CM000671.1:g.35800726A= GRCh37
NC_000009.10:g.35790726A= NCBI36
NG_009249.1:g.13321A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000448821.6:c.1239A= ENSP00000402902.2:p.Gly413=
ENST00000685871.1:c.1239A= ENSP00000509964.1:p.Gly413=
ENST00000686159.1:n.1278A=
ENST00000686486.1:n.247A=
ENST00000687302.1:n.1325A=
ENST00000687357.1:c.1239A= ENSP00000509549.1:p.Gly413=
ENST00000687625.1:n.394A=
ENST00000687787.1:c.1239A= ENSP00000509440.1:p.Gly413=
ENST00000688201.1:n.1271A=
ENST00000688226.1:n.1171A=
ENST00000688869.1:n.1545A=
ENST00000689788.1:c.1033A= ENSP00000508973.1:n.1033A=
ENST00000689898.1:c.1239A= ENSP00000509651.1:p.Gly413=
ENST00000690070.1:c.1239A= ENSP00000509654.1:p.Gly413=
ENST00000690267.1:c.1103A= ENSP00000510432.1:n.1103A=
ENST00000690552.1:n.1100A=
ENST00000691138.1:n.1100A=
ENST00000691969.1:c.814A= ENSP00000510244.1:n.814A=
ENST00000692232.1:n.2395A=
ENST00000692233.1:c.1103A= ENSP00000509698.1:n.1103A=
ENST00000692380.1:n.394A=
ENST00000692447.1:n.2351A=
ENST00000693094.1:c.1239A= ENSP00000510161.1:p.Gly413=
ENST00000342694.7:c.1239A= MANE Select ENSP00000341083.2:p.Gly413=
ENST00000342694.6:c.1239A= ENSP00000341083.2:p.Gly413=
ENST00000464810.5:n.1239A=
NM_003995.3:c.1239A= NP_003986.2:p.Gly413=
XM_005251478.3:c.1239A= XP_005251535.1:p.Gly413=
XM_005251479.3:c.252A= XP_005251536.1:p.Gly84=
XM_006716778.2:c.1239A= XP_006716841.1:p.Gly413=
XM_011517889.1:c.252A= XP_011516191.1:p.Gly84=
XM_011517890.1:c.252A= XP_011516192.1:p.Gly84=
XM_011517891.1:c.252A= XP_011516193.1:p.Gly84=
XM_011517892.1:c.252A= XP_011516194.1:p.Gly84=
XM_011517893.1:c.252A= XP_011516195.1:p.Gly84=
XM_011517894.1:c.252A= XP_011516196.1:p.Gly84=
XM_024447556.1:c.1239A= XP_024303324.1:p.Gly413=
XM_024447557.1:c.1239A= XP_024303325.1:p.Gly413=
XM_024447558.1:c.252A= XP_024303326.1:p.Gly84=
XM_024447560.1:c.-170A= XP_024303328.1:n.-170A=
XM_024447561.1:c.-170A= XP_024303329.1:n.-170A=
NM_003995.4:c.1239A= MANE Select NP_003986.2:p.Gly413=
NM_001378923.1:c.1239A= NP_001365852.1:p.Gly413=