Canonical Allele Identifier: CA2695210596

Gene: NPR2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35800775_35800782del , CM000671.2:g.35800775_35800782del	GRCh38
NC_000009.11:g.35800772_35800779del , CM000671.1:g.35800772_35800779del	GRCh37
NC_000009.10:g.35790772_35790779del	NCBI36
NG_009249.1:g.13367_13374del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000448821.6:c.1285_1292del	ENSP00000402902.2:p.Lys429SerfsTer11
ENST00000685871.1:c.1285_1292del	ENSP00000509964.1:p.Lys429SerfsTer11
ENST00000686159.1:n.1324_1331del
ENST00000686486.1:n.293_300del
ENST00000687302.1:n.1371_1378del
ENST00000687357.1:c.1285_1292del	ENSP00000509549.1:p.Lys429SerfsTer11
ENST00000687625.1:n.440_447del
ENST00000687787.1:c.1285_1292del	ENSP00000509440.1:p.Lys429SerfsTer11
ENST00000688201.1:n.1317_1324del
ENST00000688226.1:n.1217_1224del
ENST00000688869.1:n.1591_1598del
ENST00000689788.1:c.1079_1086del	ENSP00000508973.1:n.1079_1086del
ENST00000689898.1:c.1285_1292del	ENSP00000509651.1:p.Lys429SerfsTer11
ENST00000690070.1:c.1285_1292del	ENSP00000509654.1:p.Lys429SerfsTer11
ENST00000690267.1:c.1149_1156del	ENSP00000510432.1:n.1149_1156del
ENST00000690552.1:n.1146_1153del
ENST00000691138.1:n.1146_1153del
ENST00000691969.1:c.860_867del	ENSP00000510244.1:n.860_867del
ENST00000692232.1:n.2441_2448del
ENST00000692233.1:c.1149_1156del	ENSP00000509698.1:n.1149_1156del
ENST00000692380.1:n.440_447del
ENST00000692447.1:n.2397_2404del
ENST00000693094.1:c.1285_1292del	ENSP00000510161.1:p.Lys429SerfsTer11
ENST00000342694.7:c.1285_1292del MANE Select	ENSP00000341083.2:p.Lys429SerfsTer11
ENST00000342694.6:c.1285_1292del	ENSP00000341083.2:p.Lys429SerfsTer11
ENST00000464810.5:n.1285_1292del
NM_003995.3:c.1285_1292del	NP_003986.2:p.Lys429SerfsTer11
XM_005251478.3:c.1285_1292del	XP_005251535.1:p.Lys429SerfsTer11
XM_005251479.3:c.298_305del	XP_005251536.1:p.Lys100SerfsTer11
XM_006716778.2:c.1285_1292del	XP_006716841.1:p.Lys429SerfsTer11
XM_011517889.1:c.298_305del	XP_011516191.1:p.Lys100SerfsTer11
XM_011517890.1:c.298_305del	XP_011516192.1:p.Lys100SerfsTer11
XM_011517891.1:c.298_305del	XP_011516193.1:p.Lys100SerfsTer11
XM_011517892.1:c.298_305del	XP_011516194.1:p.Lys100SerfsTer11
XM_011517893.1:c.298_305del	XP_011516195.1:p.Lys100SerfsTer11
XM_011517894.1:c.298_305del	XP_011516196.1:p.Lys100SerfsTer11
XM_011517895.1:c.-124_-117del	XP_011516197.1:n.-124_-117del
XM_024447556.1:c.1285_1292del	XP_024303324.1:p.Lys429SerfsTer11
XM_024447557.1:c.1285_1292del	XP_024303325.1:p.Lys429SerfsTer11
XM_024447558.1:c.298_305del	XP_024303326.1:p.Lys100SerfsTer11
XM_024447559.1:c.-124_-117del	XP_024303327.1:n.-124_-117del
XM_024447560.1:c.-124_-117del	XP_024303328.1:n.-124_-117del
XM_024447561.1:c.-124_-117del	XP_024303329.1:n.-124_-117del
NM_003995.4:c.1285_1292del MANE Select	NP_003986.2:p.Lys429SerfsTer11
NM_001378923.1:c.1285_1292del	NP_001365852.1:p.Lys429SerfsTer11