Canonical Allele Identifier: CA373378863

Gene: NPR2

Linked Data

• MyVariant Identifiers: chr9:g.35806112A>G (hg19) ; chr9:g.35806115A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35806115A>G , CM000671.2:g.35806115A>G	GRCh38
NC_000009.11:g.35806112A>G , CM000671.1:g.35806112A>G	GRCh37
NC_000009.10:g.35796112A>G	NCBI36
NG_009249.1:g.18707A>G
NG_047141.1:g.11158T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421267.6:c.294A>G
ENST00000448821.6:c.2254A>G	ENSP00000402902.2:p.Ile752Val
ENST00000685871.1:c.2182A>G	ENSP00000509964.1:p.Ile728Val
ENST00000686159.1:n.2293A>G
ENST00000686486.1:n.1424A>G
ENST00000687302.1:n.2368A>G
ENST00000687357.1:c.2107A>G	ENSP00000509549.1:p.Ile703Val
ENST00000687625.1:n.1409A>G
ENST00000687787.1:c.2413A>G	ENSP00000509440.1:p.Ile805Val
ENST00000688201.1:n.2211A>G
ENST00000688226.1:n.2186A>G
ENST00000688869.1:n.2560A>G
ENST00000689788.1:c.2048A>G	ENSP00000508973.1:n.2048A>G
ENST00000689898.1:c.2111A>G	ENSP00000509651.1:n.2111A>G
ENST00000690070.1:c.2338A>G	ENSP00000509654.1:p.Ile780Val
ENST00000690267.1:c.2043A>G	ENSP00000510432.1:n.2043A>G
ENST00000690552.1:n.2115A>G
ENST00000691138.1:n.2043A>G
ENST00000691969.1:c.1754A>G	ENSP00000510244.1:n.1754A>G
ENST00000692232.1:n.3569A>G
ENST00000692233.1:c.2118A>G	ENSP00000509698.1:n.2118A>G
ENST00000692380.1:n.1409A>G
ENST00000692447.1:n.3370A>G
ENST00000693094.1:c.2254A>G	ENSP00000510161.1:p.Ile752Val
ENST00000342694.7:c.2254A>G MANE Select	ENSP00000341083.2:p.Ile752Val
ENST00000342694.6:c.2254A>G	ENSP00000341083.2:p.Ile752Val
ENST00000421267.5:c.294A>G
ENST00000447210.5:c.31A>G	ENSP00000393029.1:p.Ile11Val
ENST00000464810.5:n.2254A>G
NM_003995.3:c.2254A>G	NP_003986.2:p.Ile752Val
XM_005251478.3:c.2263A>G	XP_005251535.1:p.Ile755Val
XM_005251479.3:c.1276A>G	XP_005251536.1:p.Ile426Val
XM_006716778.2:c.2191A>G	XP_006716841.1:p.Ile731Val
XM_011517889.1:c.1276A>G	XP_011516191.1:p.Ile426Val
XM_011517890.1:c.1276A>G	XP_011516192.1:p.Ile426Val
XM_011517891.1:c.1276A>G	XP_011516193.1:p.Ile426Val
XM_011517892.1:c.1276A>G	XP_011516194.1:p.Ile426Val
XM_011517893.1:c.1276A>G	XP_011516195.1:p.Ile426Val
XM_011517894.1:c.1276A>G	XP_011516196.1:p.Ile426Val
XM_011517895.1:c.859A>G	XP_011516197.1:p.Ile287Val
XM_024447556.1:c.2422A>G	XP_024303324.1:p.Ile808Val
XM_024447557.1:c.2413A>G	XP_024303325.1:p.Ile805Val
XM_024447558.1:c.1435A>G	XP_024303326.1:p.Ile479Val
XM_024447559.1:c.1018A>G	XP_024303327.1:p.Ile340Val
XM_024447560.1:c.1009A>G	XP_024303328.1:p.Ile337Val
XM_024447561.1:c.850A>G	XP_024303329.1:p.Ile284Val
NM_003995.4:c.2254A>G MANE Select	NP_003986.2:p.Ile752Val
NM_001378923.1:c.2263A>G	NP_001365852.1:p.Ile755Val