Canonical Allele Identifier: CA373379188

Gene: NPR2

Linked Data

• MyVariant Identifiers: chr9:g.35806170A>G (hg19) ; chr9:g.35806173A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35806173A>G , CM000671.2:g.35806173A>G	GRCh38
NC_000009.11:g.35806170A>G , CM000671.1:g.35806170A>G	GRCh37
NC_000009.10:g.35796170A>G	NCBI36
NG_009249.1:g.18765A>G
NG_047141.1:g.11100T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421267.6:c.352A>G
ENST00000448821.6:c.2312A>G	ENSP00000402902.2:p.Gln771Arg
ENST00000685871.1:c.2240A>G	ENSP00000509964.1:p.Gln747Arg
ENST00000686159.1:n.2351A>G
ENST00000686486.1:n.1482A>G
ENST00000687302.1:n.2426A>G
ENST00000687357.1:c.2165A>G	ENSP00000509549.1:p.Gln722Arg
ENST00000687625.1:n.1467A>G
ENST00000687787.1:c.2471A>G	ENSP00000509440.1:p.Gln824Arg
ENST00000688201.1:n.2269A>G
ENST00000688226.1:n.2244A>G
ENST00000688869.1:n.2618A>G
ENST00000689788.1:c.2106A>G	ENSP00000508973.1:n.2106A>G
ENST00000689898.1:c.2169A>G	ENSP00000509651.1:n.2169A>G
ENST00000690070.1:c.2396A>G	ENSP00000509654.1:p.Gln799Arg
ENST00000690267.1:c.2101A>G	ENSP00000510432.1:n.2101A>G
ENST00000690552.1:n.2173A>G
ENST00000691138.1:n.2101A>G
ENST00000691969.1:c.1812A>G	ENSP00000510244.1:n.1812A>G
ENST00000692232.1:n.3627A>G
ENST00000692233.1:c.2176A>G	ENSP00000509698.1:n.2176A>G
ENST00000692380.1:n.1467A>G
ENST00000692447.1:n.3428A>G
ENST00000693094.1:c.2312A>G	ENSP00000510161.1:p.Gln771Arg
ENST00000342694.7:c.2312A>G MANE Select	ENSP00000341083.2:p.Gln771Arg
ENST00000342694.6:c.2312A>G	ENSP00000341083.2:p.Gln771Arg
ENST00000421267.5:c.352A>G
ENST00000447210.5:c.89A>G	ENSP00000393029.1:p.Gln30Arg
ENST00000464810.5:n.2312A>G
NM_003995.3:c.2312A>G	NP_003986.2:p.Gln771Arg
XM_005251478.3:c.2321A>G	XP_005251535.1:p.Gln774Arg
XM_005251479.3:c.1334A>G	XP_005251536.1:p.Gln445Arg
XM_006716778.2:c.2249A>G	XP_006716841.1:p.Gln750Arg
XM_011517889.1:c.1334A>G	XP_011516191.1:p.Gln445Arg
XM_011517890.1:c.1334A>G	XP_011516192.1:p.Gln445Arg
XM_011517891.1:c.1334A>G	XP_011516193.1:p.Gln445Arg
XM_011517892.1:c.1334A>G	XP_011516194.1:p.Gln445Arg
XM_011517893.1:c.1334A>G	XP_011516195.1:p.Gln445Arg
XM_011517894.1:c.1334A>G	XP_011516196.1:p.Gln445Arg
XM_011517895.1:c.917A>G	XP_011516197.1:p.Gln306Arg
XM_024447556.1:c.2480A>G	XP_024303324.1:p.Gln827Arg
XM_024447557.1:c.2471A>G	XP_024303325.1:p.Gln824Arg
XM_024447558.1:c.1493A>G	XP_024303326.1:p.Gln498Arg
XM_024447559.1:c.1076A>G	XP_024303327.1:p.Gln359Arg
XM_024447560.1:c.1067A>G	XP_024303328.1:p.Gln356Arg
XM_024447561.1:c.908A>G	XP_024303329.1:p.Gln303Arg
NM_003995.4:c.2312A>G MANE Select	NP_003986.2:p.Gln771Arg
NM_001378923.1:c.2321A>G	NP_001365852.1:p.Gln774Arg