Canonical Allele Identifier: CA373379376

Gene: NPR2

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421267.6:c.388A>T
ENST00000448821.6:c.2348A>T	ENSP00000402902.2:p.Lys783Met
ENST00000685871.1:c.2276A>T	ENSP00000509964.1:p.Lys759Met
ENST00000686159.1:n.2387A>T
ENST00000686486.1:n.1518A>T
ENST00000687302.1:n.2462A>T
ENST00000687357.1:c.2201A>T	ENSP00000509549.1:p.Lys734Met
ENST00000687625.1:n.1503A>T
ENST00000687787.1:c.2507A>T	ENSP00000509440.1:p.Lys836Met
ENST00000688201.1:n.2305A>T
ENST00000688226.1:n.2280A>T
ENST00000688869.1:n.2654A>T
ENST00000689788.1:c.2142A>T	ENSP00000508973.1:n.2142A>T
ENST00000689898.1:c.2205A>T	ENSP00000509651.1:n.2205A>T
ENST00000690070.1:c.2432A>T	ENSP00000509654.1:p.Lys811Met
ENST00000690267.1:c.2137A>T	ENSP00000510432.1:n.2137A>T
ENST00000690552.1:n.2209A>T
ENST00000691138.1:n.2137A>T
ENST00000691969.1:c.1848A>T	ENSP00000510244.1:n.1848A>T
ENST00000692232.1:n.3663A>T
ENST00000692233.1:c.2212A>T	ENSP00000509698.1:n.2212A>T
ENST00000692380.1:n.1503A>T
ENST00000692447.1:n.3464A>T
ENST00000693094.1:c.2348A>T	ENSP00000510161.1:p.Lys783Met
ENST00000342694.7:c.2348A>T MANE Select	ENSP00000341083.2:p.Lys783Met
ENST00000342694.6:c.2348A>T	ENSP00000341083.2:p.Lys783Met
ENST00000421267.5:c.388A>T
ENST00000447210.5:c.125A>T	ENSP00000393029.1:p.Lys42Met
ENST00000464810.5:n.2348A>T
NM_003995.3:c.2348A>T	NP_003986.2:p.Lys783Met
XM_005251478.3:c.2357A>T	XP_005251535.1:p.Lys786Met
XM_005251479.3:c.1370A>T	XP_005251536.1:p.Lys457Met
XM_006716778.2:c.2285A>T	XP_006716841.1:p.Lys762Met
XM_011517889.1:c.1370A>T	XP_011516191.1:p.Lys457Met
XM_011517890.1:c.1370A>T	XP_011516192.1:p.Lys457Met
XM_011517891.1:c.1370A>T	XP_011516193.1:p.Lys457Met
XM_011517892.1:c.1370A>T	XP_011516194.1:p.Lys457Met
XM_011517893.1:c.1370A>T	XP_011516195.1:p.Lys457Met
XM_011517894.1:c.1370A>T	XP_011516196.1:p.Lys457Met
XM_011517895.1:c.953A>T	XP_011516197.1:p.Lys318Met
XM_024447556.1:c.2516A>T	XP_024303324.1:p.Lys839Met
XM_024447557.1:c.2507A>T	XP_024303325.1:p.Lys836Met
XM_024447558.1:c.1529A>T	XP_024303326.1:p.Lys510Met
XM_024447559.1:c.1112A>T	XP_024303327.1:p.Lys371Met
XM_024447560.1:c.1103A>T	XP_024303328.1:p.Lys368Met
XM_024447561.1:c.944A>T	XP_024303329.1:p.Lys315Met
NM_003995.4:c.2348A>T MANE Select	NP_003986.2:p.Lys783Met
NM_001378923.1:c.2357A>T	NP_001365852.1:p.Lys786Met