Canonical Allele Identifier: CA2695210600

Gene: NPR2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35806159_35806160delinsTT , CM000671.2:g.35806159_35806160delinsTT	GRCh38
NC_000009.11:g.35806156_35806157delinsTT , CM000671.1:g.35806156_35806157delinsTT	GRCh37
NC_000009.10:g.35796156_35796157delinsTT	NCBI36
NG_009249.1:g.18751_18752delinsTT
NG_047141.1:g.11113_11114delinsAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421267.6:c.338_339delinsTT
ENST00000448821.6:c.2298_2299delinsTT	ENSP00000402902.2:p.Glu766AspfsTer2
ENST00000685871.1:c.2226_2227delinsTT	ENSP00000509964.1:p.Glu742AspfsTer2
ENST00000686159.1:n.2337_2338delinsTT
ENST00000686486.1:n.1468_1469delinsTT
ENST00000687302.1:n.2412_2413delinsTT
ENST00000687357.1:c.2151_2152delinsTT	ENSP00000509549.1:p.Glu717AspfsTer2
ENST00000687625.1:n.1453_1454delinsTT
ENST00000687787.1:c.2457_2458delinsTT	ENSP00000509440.1:p.Glu819AspfsTer2
ENST00000688201.1:n.2255_2256delinsTT
ENST00000688226.1:n.2230_2231delinsTT
ENST00000688869.1:n.2604_2605delinsTT
ENST00000689788.1:c.2092_2093delinsTT	ENSP00000508973.1:n.2092_2093delinsTT
ENST00000689898.1:c.2155_2156delinsTT	ENSP00000509651.1:n.2155_2156delinsTT
ENST00000690070.1:c.2382_2383delinsTT	ENSP00000509654.1:p.Glu794AspfsTer2
ENST00000690267.1:c.2087_2088delinsTT	ENSP00000510432.1:n.2087_2088delinsTT
ENST00000690552.1:n.2159_2160delinsTT
ENST00000691138.1:n.2087_2088delinsTT
ENST00000691969.1:c.1798_1799delinsTT	ENSP00000510244.1:n.1798_1799delinsTT
ENST00000692232.1:n.3613_3614delinsTT
ENST00000692233.1:c.2162_2163delinsTT	ENSP00000509698.1:n.2162_2163delinsTT
ENST00000692380.1:n.1453_1454delinsTT
ENST00000692447.1:n.3414_3415delinsTT
ENST00000693094.1:c.2298_2299delinsTT	ENSP00000510161.1:p.Glu766AspfsTer2
ENST00000342694.7:c.2298_2299delinsTT MANE Select	ENSP00000341083.2:p.Glu766AspfsTer2
ENST00000342694.6:c.2298_2299delinsTT	ENSP00000341083.2:p.Glu766AspfsTer2
ENST00000421267.5:c.338_339delinsTT
ENST00000447210.5:c.75_76delinsTT	ENSP00000393029.1:p.Glu25AspfsTer2
ENST00000464810.5:n.2298_2299delinsTT
NM_003995.3:c.2298_2299delinsTT	NP_003986.2:p.Glu766AspfsTer2
XM_005251478.3:c.2307_2308delinsTT	XP_005251535.1:p.Glu769AspfsTer2
XM_005251479.3:c.1320_1321delinsTT	XP_005251536.1:p.Glu440AspfsTer2
XM_006716778.2:c.2235_2236delinsTT	XP_006716841.1:p.Glu745AspfsTer2
XM_011517889.1:c.1320_1321delinsTT	XP_011516191.1:p.Glu440AspfsTer2
XM_011517890.1:c.1320_1321delinsTT	XP_011516192.1:p.Glu440AspfsTer2
XM_011517891.1:c.1320_1321delinsTT	XP_011516193.1:p.Glu440AspfsTer2
XM_011517892.1:c.1320_1321delinsTT	XP_011516194.1:p.Glu440AspfsTer2
XM_011517893.1:c.1320_1321delinsTT	XP_011516195.1:p.Glu440AspfsTer2
XM_011517894.1:c.1320_1321delinsTT	XP_011516196.1:p.Glu440AspfsTer2
XM_011517895.1:c.903_904delinsTT	XP_011516197.1:p.Glu301AspfsTer2
XM_024447556.1:c.2466_2467delinsTT	XP_024303324.1:p.Glu822AspfsTer2
XM_024447557.1:c.2457_2458delinsTT	XP_024303325.1:p.Glu819AspfsTer2
XM_024447558.1:c.1479_1480delinsTT	XP_024303326.1:p.Glu493AspfsTer2
XM_024447559.1:c.1062_1063delinsTT	XP_024303327.1:p.Glu354AspfsTer2
XM_024447560.1:c.1053_1054delinsTT	XP_024303328.1:p.Glu351AspfsTer2
XM_024447561.1:c.894_895delinsTT	XP_024303329.1:p.Glu298AspfsTer2
NM_003995.4:c.2298_2299delinsTT MANE Select	NP_003986.2:p.Glu766AspfsTer2
NM_001378923.1:c.2307_2308delinsTT	NP_001365852.1:p.Glu769AspfsTer2