Canonical Allele Identifier: CA1846132389
Gene: NPR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.35800719A= , CM000671.2:g.35800719A= GRCh38
NC_000009.11:g.35800716A= , CM000671.1:g.35800716A= GRCh37
NC_000009.10:g.35790716A= NCBI36
NG_009249.1:g.13311A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000448821.6:c.1229A= ENSP00000402902.2:p.His410=
ENST00000685871.1:c.1229A= ENSP00000509964.1:p.His410=
ENST00000686159.1:n.1268A=
ENST00000686486.1:n.237A=
ENST00000687302.1:n.1315A=
ENST00000687357.1:c.1229A= ENSP00000509549.1:p.His410=
ENST00000687625.1:n.384A=
ENST00000687787.1:c.1229A= ENSP00000509440.1:p.His410=
ENST00000688201.1:n.1261A=
ENST00000688226.1:n.1161A=
ENST00000688869.1:n.1535A=
ENST00000689788.1:c.1023A= ENSP00000508973.1:n.1023A=
ENST00000689898.1:c.1229A= ENSP00000509651.1:p.His410=
ENST00000690070.1:c.1229A= ENSP00000509654.1:p.His410=
ENST00000690267.1:c.1093A= ENSP00000510432.1:n.1093A=
ENST00000690552.1:n.1090A=
ENST00000691138.1:n.1090A=
ENST00000691969.1:c.804A= ENSP00000510244.1:n.804A=
ENST00000692232.1:n.2385A=
ENST00000692233.1:c.1093A= ENSP00000509698.1:n.1093A=
ENST00000692380.1:n.384A=
ENST00000692447.1:n.2341A=
ENST00000693094.1:c.1229A= ENSP00000510161.1:p.His410=
ENST00000342694.7:c.1229A= MANE Select ENSP00000341083.2:p.His410=
ENST00000342694.6:c.1229A= ENSP00000341083.2:p.His410=
ENST00000464810.5:n.1229A=
NM_003995.3:c.1229A= NP_003986.2:p.His410=
XM_005251478.3:c.1229A= XP_005251535.1:p.His410=
XM_005251479.3:c.242A= XP_005251536.1:p.His81=
XM_006716778.2:c.1229A= XP_006716841.1:p.His410=
XM_011517889.1:c.242A= XP_011516191.1:p.His81=
XM_011517890.1:c.242A= XP_011516192.1:p.His81=
XM_011517891.1:c.242A= XP_011516193.1:p.His81=
XM_011517892.1:c.242A= XP_011516194.1:p.His81=
XM_011517893.1:c.242A= XP_011516195.1:p.His81=
XM_011517894.1:c.242A= XP_011516196.1:p.His81=
XM_024447556.1:c.1229A= XP_024303324.1:p.His410=
XM_024447557.1:c.1229A= XP_024303325.1:p.His410=
XM_024447558.1:c.242A= XP_024303326.1:p.His81=
XM_024447560.1:c.-180A= XP_024303328.1:n.-180A=
XM_024447561.1:c.-180A= XP_024303329.1:n.-180A=
NM_003995.4:c.1229A= MANE Select NP_003986.2:p.His410=
NM_001378923.1:c.1229A= NP_001365852.1:p.His410=