Canonical Allele Identifier: CA464465044

Gene: NPR2

Linked Data

• MyVariant Identifiers: chr9:g.35806222C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35806225C>G , CM000671.2:g.35806225C>G	GRCh38
NC_000009.11:g.35806222C>G , CM000671.1:g.35806222C>G	GRCh37
NC_000009.10:g.35796222C>G	NCBI36
NG_009249.1:g.18817C>G
NG_047141.1:g.11048G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421267.6:c.404C>G
ENST00000448821.6:c.2364C>G	ENSP00000402902.2:p.Arg788=
ENST00000685871.1:c.2292C>G	ENSP00000509964.1:p.Arg764=
ENST00000686159.1:n.2403C>G
ENST00000686486.1:n.1534C>G
ENST00000687302.1:n.2478C>G
ENST00000687357.1:c.2217C>G	ENSP00000509549.1:p.Arg739=
ENST00000687625.1:n.1519C>G
ENST00000687787.1:c.2523C>G	ENSP00000509440.1:p.Arg841=
ENST00000688201.1:n.2321C>G
ENST00000688226.1:n.2296C>G
ENST00000688869.1:n.2670C>G
ENST00000689788.1:c.2158C>G	ENSP00000508973.1:n.2158C>G
ENST00000689898.1:c.2221C>G	ENSP00000509651.1:n.2221C>G
ENST00000690070.1:c.2448C>G	ENSP00000509654.1:p.Arg816=
ENST00000690267.1:c.2153C>G	ENSP00000510432.1:n.2153C>G
ENST00000690552.1:n.2225C>G
ENST00000691138.1:n.2153C>G
ENST00000691969.1:c.1864C>G	ENSP00000510244.1:n.1864C>G
ENST00000692232.1:n.3679C>G
ENST00000692233.1:c.2228C>G	ENSP00000509698.1:n.2228C>G
ENST00000692380.1:n.1519C>G
ENST00000692447.1:n.3480C>G
ENST00000693094.1:c.2364C>G	ENSP00000510161.1:p.Arg788=
ENST00000342694.7:c.2364C>G MANE Select	ENSP00000341083.2:p.Arg788=
ENST00000342694.6:c.2364C>G	ENSP00000341083.2:p.Arg788=
ENST00000421267.5:c.404C>G
ENST00000447210.5:c.141C>G	ENSP00000393029.1:p.Arg47=
ENST00000464810.5:n.2364C>G
NM_003995.3:c.2364C>G	NP_003986.2:p.Arg788=
XM_005251478.3:c.2373C>G	XP_005251535.1:p.Arg791=
XM_005251479.3:c.1386C>G	XP_005251536.1:p.Arg462=
XM_006716778.2:c.2301C>G	XP_006716841.1:p.Arg767=
XM_011517889.1:c.1386C>G	XP_011516191.1:p.Arg462=
XM_011517890.1:c.1386C>G	XP_011516192.1:p.Arg462=
XM_011517891.1:c.1386C>G	XP_011516193.1:p.Arg462=
XM_011517892.1:c.1386C>G	XP_011516194.1:p.Arg462=
XM_011517893.1:c.1386C>G	XP_011516195.1:p.Arg462=
XM_011517894.1:c.1386C>G	XP_011516196.1:p.Arg462=
XM_011517895.1:c.969C>G	XP_011516197.1:p.Arg323=
XM_024447556.1:c.2532C>G	XP_024303324.1:p.Arg844=
XM_024447557.1:c.2523C>G	XP_024303325.1:p.Arg841=
XM_024447558.1:c.1545C>G	XP_024303326.1:p.Arg515=
XM_024447559.1:c.1128C>G	XP_024303327.1:p.Arg376=
XM_024447560.1:c.1119C>G	XP_024303328.1:p.Arg373=
XM_024447561.1:c.960C>G	XP_024303329.1:p.Arg320=
NM_003995.4:c.2364C>G MANE Select	NP_003986.2:p.Arg788=
NM_001378923.1:c.2373C>G	NP_001365852.1:p.Arg791=