Canonical Allele Identifier: CA5051981

Gene: NPR2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35806553C>T , CM000671.2:g.35806553C>T	GRCh38
NC_000009.11:g.35806550C>T , CM000671.1:g.35806550C>T	GRCh37
NC_000009.10:g.35796550C>T	NCBI36
NG_009249.1:g.19145C>T
NG_047141.1:g.10720G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_003995.4:c.2519+15C>T MANE Select	NP_003986.2:n.2519+15C>T
ENST00000342694.7:c.2519+15C>T MANE Select	ENSP00000341083.2:n.2519+15C>T
NM_001378923.1:c.2528+15C>T	NP_001365852.1:n.2528+15C>T
NM_003995.3:c.2519+15C>T	NP_003986.2:n.2519+15C>T
ENST00000342694.6:c.2519+15C>T	ENSP00000341083.2:n.2519+15C>T
ENST00000421267.5:c.559+15C>T
ENST00000421267.6:c.559+15C>T
ENST00000447210.5:c.296+15C>T	ENSP00000393029.1:n.296+15C>T
ENST00000448821.5:c.6+15C>T
ENST00000448821.6:c.2519+15C>T	ENSP00000402902.2:n.2519+15C>T
ENST00000464810.5:n.2519+15C>T
ENST00000685871.1:c.2447+15C>T	ENSP00000509964.1:n.2447+15C>T
ENST00000686159.1:n.2558+15C>T
ENST00000686486.1:n.1689+15C>T
ENST00000687302.1:n.2633+15C>T
ENST00000687357.1:c.2372+15C>T	ENSP00000509549.1:n.2372+15C>T
ENST00000687625.1:n.1674+15C>T
ENST00000687787.1:c.2678+15C>T	ENSP00000509440.1:n.2678+15C>T
ENST00000688201.1:n.2476+15C>T
ENST00000688226.1:n.2451+15C>T
ENST00000688869.1:n.2825+15C>T
ENST00000689788.1:c.2313+15C>T	ENSP00000508973.1:n.2313+15C>T
ENST00000689898.1:c.2376+15C>T	ENSP00000509651.1:n.2376+15C>T
ENST00000690070.1:c.2603+15C>T	ENSP00000509654.1:n.2603+15C>T
ENST00000690267.1:c.2308+15C>T	ENSP00000510432.1:n.2308+15C>T
ENST00000690552.1:n.2395C>T
ENST00000691138.1:n.2323C>T
ENST00000691969.1:c.2019+15C>T	ENSP00000510244.1:n.2019+15C>T
ENST00000692232.1:n.3834+15C>T
ENST00000692233.1:c.2383+15C>T	ENSP00000509698.1:n.2383+15C>T
ENST00000692380.1:n.1674+15C>T
ENST00000692447.1:n.3635+15C>T
ENST00000693094.1:c.2519+15C>T	ENSP00000510161.1:n.2519+15C>T
XM_005251478.3:c.2528+15C>T	XP_005251535.1:n.2528+15C>T
XM_005251479.3:c.1541+15C>T	XP_005251536.1:n.1541+15C>T
XM_006716778.2:c.2456+15C>T	XP_006716841.1:n.2456+15C>T
XM_011517889.1:c.1541+15C>T	XP_011516191.1:n.1541+15C>T
XM_011517890.1:c.1541+15C>T	XP_011516192.1:n.1541+15C>T
XM_011517891.1:c.1541+15C>T	XP_011516193.1:n.1541+15C>T
XM_011517892.1:c.1541+15C>T	XP_011516194.1:n.1541+15C>T
XM_011517893.1:c.1541+15C>T	XP_011516195.1:n.1541+15C>T
XM_011517894.1:c.1541+15C>T	XP_011516196.1:n.1541+15C>T
XM_011517895.1:c.1124+15C>T	XP_011516197.1:n.1124+15C>T
XM_024447556.1:c.2687+15C>T	XP_024303324.1:n.2687+15C>T
XM_024447557.1:c.2678+15C>T	XP_024303325.1:n.2678+15C>T
XM_024447558.1:c.1700+15C>T	XP_024303326.1:n.1700+15C>T
XM_024447559.1:c.1283+15C>T	XP_024303327.1:n.1283+15C>T
XM_024447560.1:c.1274+15C>T	XP_024303328.1:n.1274+15C>T
XM_024447561.1:c.1115+15C>T	XP_024303329.1:n.1115+15C>T