Canonical Allele Identifier: CA915758593

Gene: NPR2

Linked Data

• dbSNP Id: rs1563987571
• gnomAD v2: 9-35800924-CTG-C
• gnomAD v3: 9-35800927-CTG-C
• gnomAD v4: 9-35800927-CTG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35800930_35800931del , CM000671.2:g.35800930_35800931del	GRCh38
NC_000009.11:g.35800927_35800928del , CM000671.1:g.35800927_35800928del	GRCh37
NC_000009.10:g.35790927_35790928del	NCBI36
NG_009249.1:g.13522_13523del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000448821.6:c.1351+89_1351+90del	ENSP00000402902.2:n.1351+89_1351+90del
ENST00000685871.1:c.1351+89_1351+90del	ENSP00000509964.1:n.1351+89_1351+90del
ENST00000686159.1:n.1390+89_1390+90del
ENST00000686486.1:n.359+89_359+90del
ENST00000687302.1:n.1437+89_1437+90del
ENST00000687357.1:c.1351+89_1351+90del	ENSP00000509549.1:n.1351+89_1351+90del
ENST00000687625.1:n.506+89_506+90del
ENST00000687787.1:c.1351+89_1351+90del	ENSP00000509440.1:n.1351+89_1351+90del
ENST00000688201.1:n.1383+89_1383+90del
ENST00000688226.1:n.1283+89_1283+90del
ENST00000688869.1:n.1657+89_1657+90del
ENST00000689788.1:c.1145+89_1145+90del	ENSP00000508973.1:n.1145+89_1145+90del
ENST00000689898.1:c.1355+85_1355+86del	ENSP00000509651.1:n.1355+85_1355+86del
ENST00000690070.1:c.1351+89_1351+90del	ENSP00000509654.1:n.1351+89_1351+90del
ENST00000690267.1:c.1215+89_1215+90del	ENSP00000510432.1:n.1215+89_1215+90del
ENST00000690552.1:n.1212+89_1212+90del
ENST00000691138.1:n.1212+89_1212+90del
ENST00000691969.1:c.926+89_926+90del	ENSP00000510244.1:n.926+89_926+90del
ENST00000692232.1:n.2507+89_2507+90del
ENST00000692233.1:c.1215+89_1215+90del	ENSP00000509698.1:n.1215+89_1215+90del
ENST00000692380.1:n.506+89_506+90del
ENST00000692447.1:n.2467+85_2467+86del
ENST00000693094.1:c.1351+89_1351+90del	ENSP00000510161.1:n.1351+89_1351+90del
ENST00000342694.7:c.1351+89_1351+90del MANE Select	ENSP00000341083.2:n.1351+89_1351+90del
ENST00000342694.6:c.1351+89_1351+90del	ENSP00000341083.2:n.1351+89_1351+90del
ENST00000464810.5:n.1351+89_1351+90del
NM_003995.3:c.1351+89_1351+90del	NP_003986.2:n.1351+89_1351+90del
XM_005251478.3:c.1351+89_1351+90del	XP_005251535.1:n.1351+89_1351+90del
XM_005251479.3:c.364+89_364+90del	XP_005251536.1:n.364+89_364+90del
XM_006716778.2:c.1351+89_1351+90del	XP_006716841.1:n.1351+89_1351+90del
XM_011517889.1:c.364+89_364+90del	XP_011516191.1:n.364+89_364+90del
XM_011517890.1:c.364+89_364+90del	XP_011516192.1:n.364+89_364+90del
XM_011517891.1:c.364+89_364+90del	XP_011516193.1:n.364+89_364+90del
XM_011517892.1:c.364+89_364+90del	XP_011516194.1:n.364+89_364+90del
XM_011517893.1:c.364+89_364+90del	XP_011516195.1:n.364+89_364+90del
XM_011517894.1:c.364+89_364+90del	XP_011516196.1:n.364+89_364+90del
XM_011517895.1:c.-54+85_-54+86del	XP_011516197.1:n.-54+85_-54+86del
XM_024447556.1:c.1351+89_1351+90del	XP_024303324.1:n.1351+89_1351+90del
XM_024447557.1:c.1351+89_1351+90del	XP_024303325.1:n.1351+89_1351+90del
XM_024447558.1:c.364+89_364+90del	XP_024303326.1:n.364+89_364+90del
XM_024447559.1:c.-54+85_-54+86del	XP_024303327.1:n.-54+85_-54+86del
XM_024447560.1:c.-54+85_-54+86del	XP_024303328.1:n.-54+85_-54+86del
XM_024447561.1:c.-54+85_-54+86del	XP_024303329.1:n.-54+85_-54+86del
NM_003995.4:c.1351+89_1351+90del MANE Select	NP_003986.2:n.1351+89_1351+90del
NM_001378923.1:c.1351+89_1351+90del	NP_001365852.1:n.1351+89_1351+90del