Canonical Allele Identifier: CA2689900970

Gene: NPR2

Linked Data

• gnomAD v4: 9-35793899-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35793900del , CM000671.2:g.35793900del	GRCh38
NC_000009.11:g.35793897del , CM000671.1:g.35793897del	GRCh37
NC_000009.10:g.35783897del	NCBI36
NG_009249.1:g.6492del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000448821.6:c.670del	ENSP00000402902.2:p.Val224CysfsTer22
ENST00000685871.1:c.670del	ENSP00000509964.1:p.Val224CysfsTer22
ENST00000686159.1:n.709del
ENST00000687302.1:n.531del
ENST00000687357.1:c.670del	ENSP00000509549.1:p.Val224CysfsTer22
ENST00000687625.1:n.164+2734del
ENST00000687787.1:c.670del	ENSP00000509440.1:p.Val224CysfsTer22
ENST00000688201.1:n.702del
ENST00000688869.1:n.751del
ENST00000689788.1:c.667+825del	ENSP00000508973.1:n.667+825del
ENST00000689898.1:c.670del	ENSP00000509651.1:p.Val224CysfsTer22
ENST00000690070.1:c.670del	ENSP00000509654.1:p.Val224CysfsTer22
ENST00000690267.1:c.670del	ENSP00000510432.1:p.Val224CysfsTer22
ENST00000690552.1:n.531del
ENST00000691138.1:n.531del
ENST00000691969.1:c.448+1044del	ENSP00000510244.1:n.448+1044del
ENST00000692233.1:c.670del	ENSP00000509698.1:p.Val224CysfsTer22
ENST00000692380.1:n.164+2734del
ENST00000692447.1:n.1492del
ENST00000693094.1:c.670del	ENSP00000510161.1:p.Val224CysfsTer22
ENST00000342694.7:c.670del MANE Select	ENSP00000341083.2:p.Val224CysfsTer22
ENST00000342694.6:c.670del	ENSP00000341083.2:p.Val224CysfsTer22
ENST00000464810.5:n.670del
NM_003995.3:c.670del	NP_003986.2:p.Val224CysfsTer22
XM_005251478.3:c.670del	XP_005251535.1:p.Val224CysfsTer22
XM_005251479.3:c.-115+3560del	XP_005251536.1:n.-115+3560del
XM_006716778.2:c.670del	XP_006716841.1:p.Val224CysfsTer22
XM_011517889.1:c.-115+3560del	XP_011516191.1:n.-115+3560del
XM_011517890.1:c.-115+3560del	XP_011516192.1:n.-115+3560del
XM_011517891.1:c.-115+3560del	XP_011516193.1:n.-115+3560del
XM_011517892.1:c.-115+3560del	XP_011516194.1:n.-115+3560del
XM_011517893.1:c.-115+3560del	XP_011516195.1:n.-115+3560del
XM_011517894.1:c.-115+3560del	XP_011516196.1:n.-115+3560del
XM_024447556.1:c.670del	XP_024303324.1:p.Val224CysfsTer22
XM_024447557.1:c.670del	XP_024303325.1:p.Val224CysfsTer22
XM_024447558.1:c.-115+3560del	XP_024303326.1:n.-115+3560del
XM_024447561.1:c.-1029del	XP_024303329.1:n.-1029del
NM_003995.4:c.670del MANE Select	NP_003986.2:p.Val224CysfsTer22
NM_001378923.1:c.670del	NP_001365852.1:p.Val224CysfsTer22