Canonical Allele Identifier: CA1846146544
Gene: NPR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.35806234G= , CM000671.2:g.35806234G= GRCh38
NC_000009.11:g.35806231G= , CM000671.1:g.35806231G= GRCh37
NC_000009.10:g.35796231G= NCBI36
NG_009249.1:g.18826G=
NG_047141.1:g.11039C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000421267.6:c.412+1G=
ENST00000448821.6:c.2372+1G= ENSP00000402902.2:n.2372+1G=
ENST00000685871.1:c.2300+1G= ENSP00000509964.1:n.2300+1G=
ENST00000686159.1:n.2411+1G=
ENST00000686486.1:n.1542+1G=
ENST00000687302.1:n.2486+1G=
ENST00000687357.1:c.2225+1G= ENSP00000509549.1:n.2225+1G=
ENST00000687625.1:n.1527+1G=
ENST00000687787.1:c.2531+1G= ENSP00000509440.1:n.2531+1G=
ENST00000688201.1:n.2329+1G=
ENST00000688226.1:n.2304+1G=
ENST00000688869.1:n.2678+1G=
ENST00000689788.1:c.2166+1G= ENSP00000508973.1:n.2166+1G=
ENST00000689898.1:c.2229+1G= ENSP00000509651.1:n.2229+1G=
ENST00000690070.1:c.2456+1G= ENSP00000509654.1:n.2456+1G=
ENST00000690267.1:c.2161+1G= ENSP00000510432.1:n.2161+1G=
ENST00000690552.1:n.2233+1G=
ENST00000691138.1:n.2161+1G=
ENST00000691969.1:c.1872+1G= ENSP00000510244.1:n.1872+1G=
ENST00000692232.1:n.3687+1G=
ENST00000692233.1:c.2236+1G= ENSP00000509698.1:n.2236+1G=
ENST00000692380.1:n.1527+1G=
ENST00000692447.1:n.3488+1G=
ENST00000693094.1:c.2372+1G= ENSP00000510161.1:n.2372+1G=
ENST00000342694.7:c.2372+1G= MANE Select ENSP00000341083.2:n.2372+1G=
ENST00000342694.6:c.2372+1G= ENSP00000341083.2:n.2372+1G=
ENST00000421267.5:c.412+1G=
ENST00000447210.5:c.149+1G= ENSP00000393029.1:n.149+1G=
ENST00000464810.5:n.2372+1G=
NM_003995.3:c.2372+1G= NP_003986.2:n.2372+1G=
XM_005251478.3:c.2381+1G= XP_005251535.1:n.2381+1G=
XM_005251479.3:c.1394+1G= XP_005251536.1:n.1394+1G=
XM_006716778.2:c.2309+1G= XP_006716841.1:n.2309+1G=
XM_011517889.1:c.1394+1G= XP_011516191.1:n.1394+1G=
XM_011517890.1:c.1394+1G= XP_011516192.1:n.1394+1G=
XM_011517891.1:c.1394+1G= XP_011516193.1:n.1394+1G=
XM_011517892.1:c.1394+1G= XP_011516194.1:n.1394+1G=
XM_011517893.1:c.1394+1G= XP_011516195.1:n.1394+1G=
XM_011517894.1:c.1394+1G= XP_011516196.1:n.1394+1G=
XM_011517895.1:c.977+1G= XP_011516197.1:n.977+1G=
XM_024447556.1:c.2540+1G= XP_024303324.1:n.2540+1G=
XM_024447557.1:c.2531+1G= XP_024303325.1:n.2531+1G=
XM_024447558.1:c.1553+1G= XP_024303326.1:n.1553+1G=
XM_024447559.1:c.1136+1G= XP_024303327.1:n.1136+1G=
XM_024447560.1:c.1127+1G= XP_024303328.1:n.1127+1G=
XM_024447561.1:c.968+1G= XP_024303329.1:n.968+1G=
NM_003995.4:c.2372+1G= MANE Select NP_003986.2:n.2372+1G=
NM_001378923.1:c.2381+1G= NP_001365852.1:n.2381+1G=