Canonical Allele Identifier: CA2579335927

Gene: NPR2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35801181del , CM000671.2:g.35801181del	GRCh38
NC_000009.11:g.35801178del , CM000671.1:g.35801178del	GRCh37
NC_000009.10:g.35791178del	NCBI36
NG_009249.1:g.13773del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000448821.6:c.1436+27del	ENSP00000402902.2:n.1436+27del
ENST00000685871.1:c.1436+27del	ENSP00000509964.1:n.1436+27del
ENST00000686159.1:n.1475+27del
ENST00000686486.1:n.444+27del
ENST00000687302.1:n.1522+27del
ENST00000687357.1:c.1436+27del	ENSP00000509549.1:n.1436+27del
ENST00000687625.1:n.591+27del
ENST00000687787.1:c.1436+27del	ENSP00000509440.1:n.1436+27del
ENST00000688201.1:n.1468+27del
ENST00000688226.1:n.1368+27del
ENST00000688869.1:n.1742+27del
ENST00000689788.1:c.1230+27del	ENSP00000508973.1:n.1230+27del
ENST00000689898.1:c.1440+27del	ENSP00000509651.1:n.1440+27del
ENST00000690070.1:c.1436+27del	ENSP00000509654.1:n.1436+27del
ENST00000690267.1:c.1300+27del	ENSP00000510432.1:n.1300+27del
ENST00000690552.1:n.1297+27del
ENST00000691138.1:n.1297+27del
ENST00000691969.1:c.1011+27del	ENSP00000510244.1:n.1011+27del
ENST00000692232.1:n.2592+27del
ENST00000692233.1:c.1300+27del	ENSP00000509698.1:n.1300+27del
ENST00000692380.1:n.591+27del
ENST00000692447.1:n.2552+27del
ENST00000693094.1:c.1436+27del	ENSP00000510161.1:n.1436+27del
ENST00000342694.7:c.1436+27del MANE Select	ENSP00000341083.2:n.1436+27del
ENST00000342694.6:c.1436+27del	ENSP00000341083.2:n.1436+27del
ENST00000464810.5:n.1436+27del
NM_003995.3:c.1436+27del	NP_003986.2:n.1436+27del
XM_005251478.3:c.1436+27del	XP_005251535.1:n.1436+27del
XM_005251479.3:c.449+27del	XP_005251536.1:n.449+27del
XM_006716778.2:c.1436+27del	XP_006716841.1:n.1436+27del
XM_011517889.1:c.449+27del	XP_011516191.1:n.449+27del
XM_011517890.1:c.449+27del	XP_011516192.1:n.449+27del
XM_011517891.1:c.449+27del	XP_011516193.1:n.449+27del
XM_011517892.1:c.449+27del	XP_011516194.1:n.449+27del
XM_011517893.1:c.449+27del	XP_011516195.1:n.449+27del
XM_011517894.1:c.449+27del	XP_011516196.1:n.449+27del
XM_011517895.1:c.32+27del	XP_011516197.1:n.32+27del
XM_024447556.1:c.1436+27del	XP_024303324.1:n.1436+27del
XM_024447557.1:c.1436+27del	XP_024303325.1:n.1436+27del
XM_024447558.1:c.449+27del	XP_024303326.1:n.449+27del
XM_024447559.1:c.32+27del	XP_024303327.1:n.32+27del
XM_024447560.1:c.32+27del	XP_024303328.1:n.32+27del
XM_024447561.1:c.32+27del	XP_024303329.1:n.32+27del
NM_003995.4:c.1436+27del MANE Select	NP_003986.2:n.1436+27del
NM_001378923.1:c.1436+27del	NP_001365852.1:n.1436+27del