Canonical Allele Identifier: CA373379374

Gene: NPR2

Linked Data

• MyVariant Identifiers: chr9:g.35806206A>G (hg19) ; chr9:g.35806209A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35806209A>G , CM000671.2:g.35806209A>G	GRCh38
NC_000009.11:g.35806206A>G , CM000671.1:g.35806206A>G	GRCh37
NC_000009.10:g.35796206A>G	NCBI36
NG_009249.1:g.18801A>G
NG_047141.1:g.11064T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421267.6:c.388A>G
ENST00000448821.6:c.2348A>G	ENSP00000402902.2:p.Lys783Arg
ENST00000685871.1:c.2276A>G	ENSP00000509964.1:p.Lys759Arg
ENST00000686159.1:n.2387A>G
ENST00000686486.1:n.1518A>G
ENST00000687302.1:n.2462A>G
ENST00000687357.1:c.2201A>G	ENSP00000509549.1:p.Lys734Arg
ENST00000687625.1:n.1503A>G
ENST00000687787.1:c.2507A>G	ENSP00000509440.1:p.Lys836Arg
ENST00000688201.1:n.2305A>G
ENST00000688226.1:n.2280A>G
ENST00000688869.1:n.2654A>G
ENST00000689788.1:c.2142A>G	ENSP00000508973.1:n.2142A>G
ENST00000689898.1:c.2205A>G	ENSP00000509651.1:n.2205A>G
ENST00000690070.1:c.2432A>G	ENSP00000509654.1:p.Lys811Arg
ENST00000690267.1:c.2137A>G	ENSP00000510432.1:n.2137A>G
ENST00000690552.1:n.2209A>G
ENST00000691138.1:n.2137A>G
ENST00000691969.1:c.1848A>G	ENSP00000510244.1:n.1848A>G
ENST00000692232.1:n.3663A>G
ENST00000692233.1:c.2212A>G	ENSP00000509698.1:n.2212A>G
ENST00000692380.1:n.1503A>G
ENST00000692447.1:n.3464A>G
ENST00000693094.1:c.2348A>G	ENSP00000510161.1:p.Lys783Arg
ENST00000342694.7:c.2348A>G MANE Select	ENSP00000341083.2:p.Lys783Arg
ENST00000342694.6:c.2348A>G	ENSP00000341083.2:p.Lys783Arg
ENST00000421267.5:c.388A>G
ENST00000447210.5:c.125A>G	ENSP00000393029.1:p.Lys42Arg
ENST00000464810.5:n.2348A>G
NM_003995.3:c.2348A>G	NP_003986.2:p.Lys783Arg
XM_005251478.3:c.2357A>G	XP_005251535.1:p.Lys786Arg
XM_005251479.3:c.1370A>G	XP_005251536.1:p.Lys457Arg
XM_006716778.2:c.2285A>G	XP_006716841.1:p.Lys762Arg
XM_011517889.1:c.1370A>G	XP_011516191.1:p.Lys457Arg
XM_011517890.1:c.1370A>G	XP_011516192.1:p.Lys457Arg
XM_011517891.1:c.1370A>G	XP_011516193.1:p.Lys457Arg
XM_011517892.1:c.1370A>G	XP_011516194.1:p.Lys457Arg
XM_011517893.1:c.1370A>G	XP_011516195.1:p.Lys457Arg
XM_011517894.1:c.1370A>G	XP_011516196.1:p.Lys457Arg
XM_011517895.1:c.953A>G	XP_011516197.1:p.Lys318Arg
XM_024447556.1:c.2516A>G	XP_024303324.1:p.Lys839Arg
XM_024447557.1:c.2507A>G	XP_024303325.1:p.Lys836Arg
XM_024447558.1:c.1529A>G	XP_024303326.1:p.Lys510Arg
XM_024447559.1:c.1112A>G	XP_024303327.1:p.Lys371Arg
XM_024447560.1:c.1103A>G	XP_024303328.1:p.Lys368Arg
XM_024447561.1:c.944A>G	XP_024303329.1:p.Lys315Arg
NM_003995.4:c.2348A>G MANE Select	NP_003986.2:p.Lys783Arg
NM_001378923.1:c.2357A>G	NP_001365852.1:p.Lys786Arg