Canonical Allele Identifier: CA1846133706

Gene: NPR2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35801179_35801180delinsCT , CM000671.2:g.35801179_35801180delinsCT	GRCh38
NC_000009.11:g.35801176_35801177delinsCT , CM000671.1:g.35801176_35801177delinsCT	GRCh37
NC_000009.10:g.35791176_35791177delinsCT	NCBI36
NG_009249.1:g.13771_13772delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000448821.6:c.1436+25_1436+26delinsCT	ENSP00000402902.2:n.1436+25_1436+26delinsCT
ENST00000685871.1:c.1436+25_1436+26delinsCT	ENSP00000509964.1:n.1436+25_1436+26delinsCT
ENST00000686159.1:n.1475+25_1475+26delinsCT
ENST00000686486.1:n.444+25_444+26delinsCT
ENST00000687302.1:n.1522+25_1522+26delinsCT
ENST00000687357.1:c.1436+25_1436+26delinsCT	ENSP00000509549.1:n.1436+25_1436+26delinsCT
ENST00000687625.1:n.591+25_591+26delinsCT
ENST00000687787.1:c.1436+25_1436+26delinsCT	ENSP00000509440.1:n.1436+25_1436+26delinsCT
ENST00000688201.1:n.1468+25_1468+26delinsCT
ENST00000688226.1:n.1368+25_1368+26delinsCT
ENST00000688869.1:n.1742+25_1742+26delinsCT
ENST00000689788.1:c.1230+25_1230+26delinsCT	ENSP00000508973.1:n.1230+25_1230+26delinsCT
ENST00000689898.1:c.1440+25_1440+26delinsCT	ENSP00000509651.1:n.1440+25_1440+26delinsCT
ENST00000690070.1:c.1436+25_1436+26delinsCT	ENSP00000509654.1:n.1436+25_1436+26delinsCT
ENST00000690267.1:c.1300+25_1300+26delinsCT	ENSP00000510432.1:n.1300+25_1300+26delinsCT
ENST00000690552.1:n.1297+25_1297+26delinsCT
ENST00000691138.1:n.1297+25_1297+26delinsCT
ENST00000691969.1:c.1011+25_1011+26delinsCT	ENSP00000510244.1:n.1011+25_1011+26delinsCT
ENST00000692232.1:n.2592+25_2592+26delinsCT
ENST00000692233.1:c.1300+25_1300+26delinsCT	ENSP00000509698.1:n.1300+25_1300+26delinsCT
ENST00000692380.1:n.591+25_591+26delinsCT
ENST00000692447.1:n.2552+25_2552+26delinsCT
ENST00000693094.1:c.1436+25_1436+26delinsCT	ENSP00000510161.1:n.1436+25_1436+26delinsCT
ENST00000342694.7:c.1436+25_1436+26delinsCT MANE Select	ENSP00000341083.2:n.1436+25_1436+26delinsCT
ENST00000342694.6:c.1436+25_1436+26delinsCT	ENSP00000341083.2:n.1436+25_1436+26delinsCT
ENST00000464810.5:n.1436+25_1436+26delinsCT
NM_003995.3:c.1436+25_1436+26delinsCT	NP_003986.2:n.1436+25_1436+26delinsCT
XM_005251478.3:c.1436+25_1436+26delinsCT	XP_005251535.1:n.1436+25_1436+26delinsCT
XM_005251479.3:c.449+25_449+26delinsCT	XP_005251536.1:n.449+25_449+26delinsCT
XM_006716778.2:c.1436+25_1436+26delinsCT	XP_006716841.1:n.1436+25_1436+26delinsCT
XM_011517889.1:c.449+25_449+26delinsCT	XP_011516191.1:n.449+25_449+26delinsCT
XM_011517890.1:c.449+25_449+26delinsCT	XP_011516192.1:n.449+25_449+26delinsCT
XM_011517891.1:c.449+25_449+26delinsCT	XP_011516193.1:n.449+25_449+26delinsCT
XM_011517892.1:c.449+25_449+26delinsCT	XP_011516194.1:n.449+25_449+26delinsCT
XM_011517893.1:c.449+25_449+26delinsCT	XP_011516195.1:n.449+25_449+26delinsCT
XM_011517894.1:c.449+25_449+26delinsCT	XP_011516196.1:n.449+25_449+26delinsCT
XM_011517895.1:c.32+25_32+26delinsCT	XP_011516197.1:n.32+25_32+26delinsCT
XM_024447556.1:c.1436+25_1436+26delinsCT	XP_024303324.1:n.1436+25_1436+26delinsCT
XM_024447557.1:c.1436+25_1436+26delinsCT	XP_024303325.1:n.1436+25_1436+26delinsCT
XM_024447558.1:c.449+25_449+26delinsCT	XP_024303326.1:n.449+25_449+26delinsCT
XM_024447559.1:c.32+25_32+26delinsCT	XP_024303327.1:n.32+25_32+26delinsCT
XM_024447560.1:c.32+25_32+26delinsCT	XP_024303328.1:n.32+25_32+26delinsCT
XM_024447561.1:c.32+25_32+26delinsCT	XP_024303329.1:n.32+25_32+26delinsCT
NM_003995.4:c.1436+25_1436+26delinsCT MANE Select	NP_003986.2:n.1436+25_1436+26delinsCT
NM_001378923.1:c.1436+25_1436+26delinsCT	NP_001365852.1:n.1436+25_1436+26delinsCT