Canonical Allele Identifier: CA2689898259

Gene: NPR2

Linked Data

• gnomAD v4: 9-35806244-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35806244A>G , CM000671.2:g.35806244A>G	GRCh38
NC_000009.11:g.35806241A>G , CM000671.1:g.35806241A>G	GRCh37
NC_000009.10:g.35796241A>G	NCBI36
NG_009249.1:g.18836A>G
NG_047141.1:g.11029T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421267.6:c.412+11A>G
ENST00000448821.6:c.2372+11A>G	ENSP00000402902.2:n.2372+11A>G
ENST00000685871.1:c.2300+11A>G	ENSP00000509964.1:n.2300+11A>G
ENST00000686159.1:n.2411+11A>G
ENST00000686486.1:n.1542+11A>G
ENST00000687302.1:n.2486+11A>G
ENST00000687357.1:c.2225+11A>G	ENSP00000509549.1:n.2225+11A>G
ENST00000687625.1:n.1527+11A>G
ENST00000687787.1:c.2531+11A>G	ENSP00000509440.1:n.2531+11A>G
ENST00000688201.1:n.2329+11A>G
ENST00000688226.1:n.2304+11A>G
ENST00000688869.1:n.2678+11A>G
ENST00000689788.1:c.2166+11A>G	ENSP00000508973.1:n.2166+11A>G
ENST00000689898.1:c.2229+11A>G	ENSP00000509651.1:n.2229+11A>G
ENST00000690070.1:c.2456+11A>G	ENSP00000509654.1:n.2456+11A>G
ENST00000690267.1:c.2161+11A>G	ENSP00000510432.1:n.2161+11A>G
ENST00000690552.1:n.2233+11A>G
ENST00000691138.1:n.2161+11A>G
ENST00000691969.1:c.1872+11A>G	ENSP00000510244.1:n.1872+11A>G
ENST00000692232.1:n.3687+11A>G
ENST00000692233.1:c.2236+11A>G	ENSP00000509698.1:n.2236+11A>G
ENST00000692380.1:n.1527+11A>G
ENST00000692447.1:n.3488+11A>G
ENST00000693094.1:c.2372+11A>G	ENSP00000510161.1:n.2372+11A>G
ENST00000342694.7:c.2372+11A>G MANE Select	ENSP00000341083.2:n.2372+11A>G
ENST00000342694.6:c.2372+11A>G	ENSP00000341083.2:n.2372+11A>G
ENST00000421267.5:c.412+11A>G
ENST00000447210.5:c.149+11A>G	ENSP00000393029.1:n.149+11A>G
ENST00000464810.5:n.2372+11A>G
NM_003995.3:c.2372+11A>G	NP_003986.2:n.2372+11A>G
XM_005251478.3:c.2381+11A>G	XP_005251535.1:n.2381+11A>G
XM_005251479.3:c.1394+11A>G	XP_005251536.1:n.1394+11A>G
XM_006716778.2:c.2309+11A>G	XP_006716841.1:n.2309+11A>G
XM_011517889.1:c.1394+11A>G	XP_011516191.1:n.1394+11A>G
XM_011517890.1:c.1394+11A>G	XP_011516192.1:n.1394+11A>G
XM_011517891.1:c.1394+11A>G	XP_011516193.1:n.1394+11A>G
XM_011517892.1:c.1394+11A>G	XP_011516194.1:n.1394+11A>G
XM_011517893.1:c.1394+11A>G	XP_011516195.1:n.1394+11A>G
XM_011517894.1:c.1394+11A>G	XP_011516196.1:n.1394+11A>G
XM_011517895.1:c.977+11A>G	XP_011516197.1:n.977+11A>G
XM_024447556.1:c.2540+11A>G	XP_024303324.1:n.2540+11A>G
XM_024447557.1:c.2531+11A>G	XP_024303325.1:n.2531+11A>G
XM_024447558.1:c.1553+11A>G	XP_024303326.1:n.1553+11A>G
XM_024447559.1:c.1136+11A>G	XP_024303327.1:n.1136+11A>G
XM_024447560.1:c.1127+11A>G	XP_024303328.1:n.1127+11A>G
XM_024447561.1:c.968+11A>G	XP_024303329.1:n.968+11A>G
NM_003995.4:c.2372+11A>G MANE Select	NP_003986.2:n.2372+11A>G
NM_001378923.1:c.2381+11A>G	NP_001365852.1:n.2381+11A>G