Canonical Allele Identifier: CA1846132312

Gene: NPR2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35800702_35800703delinsCT , CM000671.2:g.35800702_35800703delinsCT	GRCh38
NC_000009.11:g.35800699_35800700delinsCT , CM000671.1:g.35800699_35800700delinsCT	GRCh37
NC_000009.10:g.35790699_35790700delinsCT	NCBI36
NG_009249.1:g.13294_13295delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000448821.6:c.1219-7_1219-6delinsCT	ENSP00000402902.2:n.1219-7_1219-6delinsCT
ENST00000685871.1:c.1219-7_1219-6delinsCT	ENSP00000509964.1:n.1219-7_1219-6delinsCT
ENST00000686159.1:n.1258-7_1258-6delinsCT
ENST00000686486.1:n.220_221delinsCT
ENST00000687302.1:n.1298_1299delinsCT
ENST00000687357.1:c.1219-7_1219-6delinsCT	ENSP00000509549.1:n.1219-7_1219-6delinsCT
ENST00000687625.1:n.374-7_374-6delinsCT
ENST00000687787.1:c.1219-7_1219-6delinsCT	ENSP00000509440.1:n.1219-7_1219-6delinsCT
ENST00000688201.1:n.1251-7_1251-6delinsCT
ENST00000688226.1:n.1151-7_1151-6delinsCT
ENST00000688869.1:n.1518_1519delinsCT
ENST00000689788.1:c.1013-7_1013-6delinsCT	ENSP00000508973.1:n.1013-7_1013-6delinsCT
ENST00000689898.1:c.1219-7_1219-6delinsCT	ENSP00000509651.1:n.1219-7_1219-6delinsCT
ENST00000690070.1:c.1219-7_1219-6delinsCT	ENSP00000509654.1:n.1219-7_1219-6delinsCT
ENST00000690267.1:c.1083-7_1083-6delinsCT	ENSP00000510432.1:n.1083-7_1083-6delinsCT
ENST00000690552.1:n.1080-7_1080-6delinsCT
ENST00000691138.1:n.1080-7_1080-6delinsCT
ENST00000691969.1:c.794-7_794-6delinsCT	ENSP00000510244.1:n.794-7_794-6delinsCT
ENST00000692232.1:n.2368_2369delinsCT
ENST00000692233.1:c.1083-7_1083-6delinsCT	ENSP00000509698.1:n.1083-7_1083-6delinsCT
ENST00000692380.1:n.374-7_374-6delinsCT
ENST00000692447.1:n.2331-7_2331-6delinsCT
ENST00000693094.1:c.1219-7_1219-6delinsCT	ENSP00000510161.1:n.1219-7_1219-6delinsCT
ENST00000342694.7:c.1219-7_1219-6delinsCT MANE Select	ENSP00000341083.2:n.1219-7_1219-6delinsCT
ENST00000342694.6:c.1219-7_1219-6delinsCT	ENSP00000341083.2:n.1219-7_1219-6delinsCT
ENST00000464810.5:n.1219-7_1219-6delinsCT
NM_003995.3:c.1219-7_1219-6delinsCT	NP_003986.2:n.1219-7_1219-6delinsCT
XM_005251478.3:c.1219-7_1219-6delinsCT	XP_005251535.1:n.1219-7_1219-6delinsCT
XM_005251479.3:c.232-7_232-6delinsCT	XP_005251536.1:n.232-7_232-6delinsCT
XM_006716778.2:c.1219-7_1219-6delinsCT	XP_006716841.1:n.1219-7_1219-6delinsCT
XM_011517889.1:c.232-7_232-6delinsCT	XP_011516191.1:n.232-7_232-6delinsCT
XM_011517890.1:c.232-7_232-6delinsCT	XP_011516192.1:n.232-7_232-6delinsCT
XM_011517891.1:c.232-7_232-6delinsCT	XP_011516193.1:n.232-7_232-6delinsCT
XM_011517892.1:c.232-7_232-6delinsCT	XP_011516194.1:n.232-7_232-6delinsCT
XM_011517893.1:c.232-7_232-6delinsCT	XP_011516195.1:n.232-7_232-6delinsCT
XM_011517894.1:c.232-7_232-6delinsCT	XP_011516196.1:n.232-7_232-6delinsCT
XM_024447556.1:c.1219-7_1219-6delinsCT	XP_024303324.1:n.1219-7_1219-6delinsCT
XM_024447557.1:c.1219-7_1219-6delinsCT	XP_024303325.1:n.1219-7_1219-6delinsCT
XM_024447558.1:c.232-7_232-6delinsCT	XP_024303326.1:n.232-7_232-6delinsCT
XM_024447560.1:c.-190-7_-190-6delinsCT	XP_024303328.1:n.-190-7_-190-6delinsCT
XM_024447561.1:c.-190-7_-190-6delinsCT	XP_024303329.1:n.-190-7_-190-6delinsCT
NM_003995.4:c.1219-7_1219-6delinsCT MANE Select	NP_003986.2:n.1219-7_1219-6delinsCT
NM_001378923.1:c.1219-7_1219-6delinsCT	NP_001365852.1:n.1219-7_1219-6delinsCT