Canonical Allele Identifier: CA464615540

Gene: NPR2

Linked Data

• MyVariant Identifiers: chr9:g.35806087T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35806090T>A , CM000671.2:g.35806090T>A	GRCh38
NC_000009.11:g.35806087T>A , CM000671.1:g.35806087T>A	GRCh37
NC_000009.10:g.35796087T>A	NCBI36
NG_009249.1:g.18682T>A
NG_047141.1:g.11183A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421267.6:c.269T>A
ENST00000448821.6:c.2229T>A	ENSP00000402902.2:p.Gly743=
ENST00000685871.1:c.2157T>A	ENSP00000509964.1:p.Gly719=
ENST00000686159.1:n.2268T>A
ENST00000686486.1:n.1399T>A
ENST00000687302.1:n.2343T>A
ENST00000687357.1:c.2082T>A	ENSP00000509549.1:p.Gly694=
ENST00000687625.1:n.1384T>A
ENST00000687787.1:c.2388T>A	ENSP00000509440.1:p.Gly796=
ENST00000688201.1:n.2186T>A
ENST00000688226.1:n.2161T>A
ENST00000688869.1:n.2535T>A
ENST00000689788.1:c.2023T>A	ENSP00000508973.1:n.2023T>A
ENST00000689898.1:c.2086T>A	ENSP00000509651.1:n.2086T>A
ENST00000690070.1:c.2313T>A	ENSP00000509654.1:p.Gly771=
ENST00000690267.1:c.2018T>A	ENSP00000510432.1:n.2018T>A
ENST00000690552.1:n.2090T>A
ENST00000691138.1:n.2018T>A
ENST00000691969.1:c.1729T>A	ENSP00000510244.1:n.1729T>A
ENST00000692232.1:n.3544T>A
ENST00000692233.1:c.2093T>A	ENSP00000509698.1:n.2093T>A
ENST00000692380.1:n.1384T>A
ENST00000692447.1:n.3345T>A
ENST00000693094.1:c.2229T>A	ENSP00000510161.1:p.Gly743=
ENST00000342694.7:c.2229T>A MANE Select	ENSP00000341083.2:p.Gly743=
ENST00000342694.6:c.2229T>A	ENSP00000341083.2:p.Gly743=
ENST00000421267.5:c.269T>A
ENST00000447210.5:c.6T>A	ENSP00000393029.1:p.Gly2=
ENST00000464810.5:n.2229T>A
NM_003995.3:c.2229T>A	NP_003986.2:p.Gly743=
XM_005251478.3:c.2238T>A	XP_005251535.1:p.Gly746=
XM_005251479.3:c.1251T>A	XP_005251536.1:p.Gly417=
XM_006716778.2:c.2166T>A	XP_006716841.1:p.Gly722=
XM_011517889.1:c.1251T>A	XP_011516191.1:p.Gly417=
XM_011517890.1:c.1251T>A	XP_011516192.1:p.Gly417=
XM_011517891.1:c.1251T>A	XP_011516193.1:p.Gly417=
XM_011517892.1:c.1251T>A	XP_011516194.1:p.Gly417=
XM_011517893.1:c.1251T>A	XP_011516195.1:p.Gly417=
XM_011517894.1:c.1251T>A	XP_011516196.1:p.Gly417=
XM_011517895.1:c.834T>A	XP_011516197.1:p.Gly278=
XM_024447556.1:c.2397T>A	XP_024303324.1:p.Gly799=
XM_024447557.1:c.2388T>A	XP_024303325.1:p.Gly796=
XM_024447558.1:c.1410T>A	XP_024303326.1:p.Gly470=
XM_024447559.1:c.993T>A	XP_024303327.1:p.Gly331=
XM_024447560.1:c.984T>A	XP_024303328.1:p.Gly328=
XM_024447561.1:c.825T>A	XP_024303329.1:p.Gly275=
NM_003995.4:c.2229T>A MANE Select	NP_003986.2:p.Gly743=
NM_001378923.1:c.2238T>A	NP_001365852.1:p.Gly746=