Canonical Allele Identifier: CA464465039

Gene: NPR2

Linked Data

• MyVariant Identifiers: chr9:g.35806219G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35806222G>T , CM000671.2:g.35806222G>T	GRCh38
NC_000009.11:g.35806219G>T , CM000671.1:g.35806219G>T	GRCh37
NC_000009.10:g.35796219G>T	NCBI36
NG_009249.1:g.18814G>T
NG_047141.1:g.11051C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421267.6:c.401G>T
ENST00000448821.6:c.2361G>T	ENSP00000402902.2:p.Arg787=
ENST00000685871.1:c.2289G>T	ENSP00000509964.1:p.Arg763=
ENST00000686159.1:n.2400G>T
ENST00000686486.1:n.1531G>T
ENST00000687302.1:n.2475G>T
ENST00000687357.1:c.2214G>T	ENSP00000509549.1:p.Arg738=
ENST00000687625.1:n.1516G>T
ENST00000687787.1:c.2520G>T	ENSP00000509440.1:p.Arg840=
ENST00000688201.1:n.2318G>T
ENST00000688226.1:n.2293G>T
ENST00000688869.1:n.2667G>T
ENST00000689788.1:c.2155G>T	ENSP00000508973.1:n.2155G>T
ENST00000689898.1:c.2218G>T	ENSP00000509651.1:n.2218G>T
ENST00000690070.1:c.2445G>T	ENSP00000509654.1:p.Arg815=
ENST00000690267.1:c.2150G>T	ENSP00000510432.1:n.2150G>T
ENST00000690552.1:n.2222G>T
ENST00000691138.1:n.2150G>T
ENST00000691969.1:c.1861G>T	ENSP00000510244.1:n.1861G>T
ENST00000692232.1:n.3676G>T
ENST00000692233.1:c.2225G>T	ENSP00000509698.1:n.2225G>T
ENST00000692380.1:n.1516G>T
ENST00000692447.1:n.3477G>T
ENST00000693094.1:c.2361G>T	ENSP00000510161.1:p.Arg787=
ENST00000342694.7:c.2361G>T MANE Select	ENSP00000341083.2:p.Arg787=
ENST00000342694.6:c.2361G>T	ENSP00000341083.2:p.Arg787=
ENST00000421267.5:c.401G>T
ENST00000447210.5:c.138G>T	ENSP00000393029.1:p.Arg46=
ENST00000464810.5:n.2361G>T
NM_003995.3:c.2361G>T	NP_003986.2:p.Arg787=
XM_005251478.3:c.2370G>T	XP_005251535.1:p.Arg790=
XM_005251479.3:c.1383G>T	XP_005251536.1:p.Arg461=
XM_006716778.2:c.2298G>T	XP_006716841.1:p.Arg766=
XM_011517889.1:c.1383G>T	XP_011516191.1:p.Arg461=
XM_011517890.1:c.1383G>T	XP_011516192.1:p.Arg461=
XM_011517891.1:c.1383G>T	XP_011516193.1:p.Arg461=
XM_011517892.1:c.1383G>T	XP_011516194.1:p.Arg461=
XM_011517893.1:c.1383G>T	XP_011516195.1:p.Arg461=
XM_011517894.1:c.1383G>T	XP_011516196.1:p.Arg461=
XM_011517895.1:c.966G>T	XP_011516197.1:p.Arg322=
XM_024447556.1:c.2529G>T	XP_024303324.1:p.Arg843=
XM_024447557.1:c.2520G>T	XP_024303325.1:p.Arg840=
XM_024447558.1:c.1542G>T	XP_024303326.1:p.Arg514=
XM_024447559.1:c.1125G>T	XP_024303327.1:p.Arg375=
XM_024447560.1:c.1116G>T	XP_024303328.1:p.Arg372=
XM_024447561.1:c.957G>T	XP_024303329.1:p.Arg319=
NM_003995.4:c.2361G>T MANE Select	NP_003986.2:p.Arg787=
NM_001378923.1:c.2370G>T	NP_001365852.1:p.Arg790=