Canonical Allele Identifier: CA373379115

Gene: NPR2

Linked Data

• MyVariant Identifiers: chr9:g.35806155A>T (hg19) ; chr9:g.35806158A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35806158A>T , CM000671.2:g.35806158A>T	GRCh38
NC_000009.11:g.35806155A>T , CM000671.1:g.35806155A>T	GRCh37
NC_000009.10:g.35796155A>T	NCBI36
NG_009249.1:g.18750A>T
NG_047141.1:g.11115T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421267.6:c.337A>T
ENST00000448821.6:c.2297A>T	ENSP00000402902.2:p.Glu766Val
ENST00000685871.1:c.2225A>T	ENSP00000509964.1:p.Glu742Val
ENST00000686159.1:n.2336A>T
ENST00000686486.1:n.1467A>T
ENST00000687302.1:n.2411A>T
ENST00000687357.1:c.2150A>T	ENSP00000509549.1:p.Glu717Val
ENST00000687625.1:n.1452A>T
ENST00000687787.1:c.2456A>T	ENSP00000509440.1:p.Glu819Val
ENST00000688201.1:n.2254A>T
ENST00000688226.1:n.2229A>T
ENST00000688869.1:n.2603A>T
ENST00000689788.1:c.2091A>T	ENSP00000508973.1:n.2091A>T
ENST00000689898.1:c.2154A>T	ENSP00000509651.1:n.2154A>T
ENST00000690070.1:c.2381A>T	ENSP00000509654.1:p.Glu794Val
ENST00000690267.1:c.2086A>T	ENSP00000510432.1:n.2086A>T
ENST00000690552.1:n.2158A>T
ENST00000691138.1:n.2086A>T
ENST00000691969.1:c.1797A>T	ENSP00000510244.1:n.1797A>T
ENST00000692232.1:n.3612A>T
ENST00000692233.1:c.2161A>T	ENSP00000509698.1:n.2161A>T
ENST00000692380.1:n.1452A>T
ENST00000692447.1:n.3413A>T
ENST00000693094.1:c.2297A>T	ENSP00000510161.1:p.Glu766Val
ENST00000342694.7:c.2297A>T MANE Select	ENSP00000341083.2:p.Glu766Val
ENST00000342694.6:c.2297A>T	ENSP00000341083.2:p.Glu766Val
ENST00000421267.5:c.337A>T
ENST00000447210.5:c.74A>T	ENSP00000393029.1:p.Glu25Val
ENST00000464810.5:n.2297A>T
NM_003995.3:c.2297A>T	NP_003986.2:p.Glu766Val
XM_005251478.3:c.2306A>T	XP_005251535.1:p.Glu769Val
XM_005251479.3:c.1319A>T	XP_005251536.1:p.Glu440Val
XM_006716778.2:c.2234A>T	XP_006716841.1:p.Glu745Val
XM_011517889.1:c.1319A>T	XP_011516191.1:p.Glu440Val
XM_011517890.1:c.1319A>T	XP_011516192.1:p.Glu440Val
XM_011517891.1:c.1319A>T	XP_011516193.1:p.Glu440Val
XM_011517892.1:c.1319A>T	XP_011516194.1:p.Glu440Val
XM_011517893.1:c.1319A>T	XP_011516195.1:p.Glu440Val
XM_011517894.1:c.1319A>T	XP_011516196.1:p.Glu440Val
XM_011517895.1:c.902A>T	XP_011516197.1:p.Glu301Val
XM_024447556.1:c.2465A>T	XP_024303324.1:p.Glu822Val
XM_024447557.1:c.2456A>T	XP_024303325.1:p.Glu819Val
XM_024447558.1:c.1478A>T	XP_024303326.1:p.Glu493Val
XM_024447559.1:c.1061A>T	XP_024303327.1:p.Glu354Val
XM_024447560.1:c.1052A>T	XP_024303328.1:p.Glu351Val
XM_024447561.1:c.893A>T	XP_024303329.1:p.Glu298Val
NM_003995.4:c.2297A>T MANE Select	NP_003986.2:p.Glu766Val
NM_001378923.1:c.2306A>T	NP_001365852.1:p.Glu769Val