Canonical Allele Identifier: CA1846154017

Gene: NPR2 SPAG8

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35808811G= , CM000671.2:g.35808811G=	GRCh38
NC_000009.11:g.35808808G= , CM000671.1:g.35808808G=	GRCh37
NC_000009.10:g.35798808G=	NCBI36
NG_009249.1:g.21403G=
NG_047141.1:g.8462C=

Transcript Alleles

HGVS	Amino-acid Change
NM_003995.4:c.2944G= (NPR2) MANE Select	NP_003986.2:p.Asp982=
ENST00000342694.7:c.2944G= (NPR2) MANE Select	ENSP00000341083.2:p.Asp982=
NM_001366760.2:c.1201-505C= (SPAG8)	NP_001353689.1:n.1201-505C=
NM_001378923.1:c.2953G= (NPR2)	NP_001365852.1:p.Asp985=
NM_003995.3:c.2944G= (NPR2)	NP_003986.2:p.Asp982=
NM_172312.1:c.1373-505C= (SPAG8)	NP_758516.1:n.1373-505C=
NM_172312.2:c.1373-505C= (SPAG8)	NP_758516.1:n.1373-505C=
NR_159431.2:n.1303-505C= (SPAG8)
ENST00000340291.6:c.1373-505C= (SPAG8)	ENSP00000340982.2:n.1373-505C=
ENST00000342694.6:c.2944G= (NPR2)	ENSP00000341083.2:p.Asp982=
ENST00000421267.6:c.984G= (NPR2)
ENST00000447210.5:c.483-841G= (NPR2)	ENSP00000393029.1:n.483-841G=
ENST00000448821.5:c.256G= (NPR2)
ENST00000448821.6:c.2769G= (NPR2)	ENSP00000402902.2:n.2769G=
ENST00000460836.5:n.417-505C= (SPAG8)
ENST00000463889.5:n.467-505C= (SPAG8)
ENST00000464810.5:n.3015G= (NPR2)
ENST00000469249.1:n.411G= (NPR2)
ENST00000475644.5:c.*826-505C= (SPAG8)	ENSP00000418530.1:n.*826-505C=
ENST00000489063.1:n.475-505C= (SPAG8)
ENST00000685871.1:c.2872G= (NPR2)	ENSP00000509964.1:p.Asp958=
ENST00000686159.1:n.2983G= (NPR2)
ENST00000686486.1:n.2185G= (NPR2)
ENST00000687302.1:n.3129G= (NPR2)
ENST00000687357.1:c.2797G= (NPR2)	ENSP00000509549.1:p.Asp933=
ENST00000687625.1:n.2099G= (NPR2)
ENST00000687787.1:c.3103G= (NPR2)	ENSP00000509440.1:p.Asp1035=
ENST00000688201.1:n.2901G= (NPR2)
ENST00000688226.1:n.2876G= (NPR2)
ENST00000688869.1:n.3250G= (NPR2)
ENST00000689788.1:c.2738G= (NPR2)	ENSP00000508973.1:n.2738G=
ENST00000689898.1:c.2801G= (NPR2)	ENSP00000509651.1:n.2801G=
ENST00000690070.1:c.3028G= (NPR2)	ENSP00000509654.1:p.Asp1010=
ENST00000690267.1:c.2733G= (NPR2)	ENSP00000510432.1:n.2733G=
ENST00000690552.1:n.3289G= (NPR2)
ENST00000691138.1:n.3288G= (NPR2)
ENST00000691969.1:c.2444G= (NPR2)	ENSP00000510244.1:n.2444G=
ENST00000692232.1:n.4259G= (NPR2)
ENST00000692233.1:c.2808G= (NPR2)	ENSP00000509698.1:n.2808G=
ENST00000692380.1:n.2099G= (NPR2)
ENST00000692447.1:n.4060G= (NPR2)
ENST00000693094.1:c.3034G= (NPR2)	ENSP00000510161.1:p.Asp1012=
XM_005251438.1:c.1201-505C= (SPAG8)	XP_005251495.1:n.1201-505C=
XM_005251478.3:c.2953G= (NPR2)	XP_005251535.1:p.Asp985=
XM_005251479.3:c.1966G= (NPR2)	XP_005251536.1:p.Asp656=
XM_006716778.2:c.2881G= (NPR2)	XP_006716841.1:p.Asp961=
XM_011517889.1:c.1966G= (NPR2)	XP_011516191.1:p.Asp656=
XM_011517890.1:c.1966G= (NPR2)	XP_011516192.1:p.Asp656=
XM_011517891.1:c.1966G= (NPR2)	XP_011516193.1:p.Asp656=
XM_011517892.1:c.1966G= (NPR2)	XP_011516194.1:p.Asp656=
XM_011517893.1:c.1966G= (NPR2)	XP_011516195.1:p.Asp656=
XM_011517894.1:c.1966G= (NPR2)	XP_011516196.1:p.Asp656=
XM_011517895.1:c.1549G= (NPR2)	XP_011516197.1:p.Asp517=
XM_024447512.1:c.1210-505C= (SPAG8)	XP_024303280.1:n.1210-505C=
XM_024447513.1:c.1201-505C= (SPAG8)	XP_024303281.1:n.1201-505C=
XM_024447556.1:c.3112G= (NPR2)	XP_024303324.1:p.Asp1038=
XM_024447557.1:c.3103G= (NPR2)	XP_024303325.1:p.Asp1035=
XM_024447558.1:c.2125G= (NPR2)	XP_024303326.1:p.Asp709=
XM_024447559.1:c.1708G= (NPR2)	XP_024303327.1:p.Asp570=
XM_024447560.1:c.1699G= (NPR2)	XP_024303328.1:p.Asp567=
XM_024447561.1:c.1540G= (NPR2)	XP_024303329.1:p.Asp514=
XR_002956772.1:n.1313-505C= (SPAG8)