Canonical Allele Identifier: CA373379356

Gene: NPR2

Linked Data

• MyVariant Identifiers: chr9:g.35806203T>A (hg19) ; chr9:g.35806206T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35806206T>A , CM000671.2:g.35806206T>A	GRCh38
NC_000009.11:g.35806203T>A , CM000671.1:g.35806203T>A	GRCh37
NC_000009.10:g.35796203T>A	NCBI36
NG_009249.1:g.18798T>A
NG_047141.1:g.11067A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421267.6:c.385T>A
ENST00000448821.6:c.2345T>A	ENSP00000402902.2:p.Ile782Asn
ENST00000685871.1:c.2273T>A	ENSP00000509964.1:p.Ile758Asn
ENST00000686159.1:n.2384T>A
ENST00000686486.1:n.1515T>A
ENST00000687302.1:n.2459T>A
ENST00000687357.1:c.2198T>A	ENSP00000509549.1:p.Ile733Asn
ENST00000687625.1:n.1500T>A
ENST00000687787.1:c.2504T>A	ENSP00000509440.1:p.Ile835Asn
ENST00000688201.1:n.2302T>A
ENST00000688226.1:n.2277T>A
ENST00000688869.1:n.2651T>A
ENST00000689788.1:c.2139T>A	ENSP00000508973.1:n.2139T>A
ENST00000689898.1:c.2202T>A	ENSP00000509651.1:n.2202T>A
ENST00000690070.1:c.2429T>A	ENSP00000509654.1:p.Ile810Asn
ENST00000690267.1:c.2134T>A	ENSP00000510432.1:n.2134T>A
ENST00000690552.1:n.2206T>A
ENST00000691138.1:n.2134T>A
ENST00000691969.1:c.1845T>A	ENSP00000510244.1:n.1845T>A
ENST00000692232.1:n.3660T>A
ENST00000692233.1:c.2209T>A	ENSP00000509698.1:n.2209T>A
ENST00000692380.1:n.1500T>A
ENST00000692447.1:n.3461T>A
ENST00000693094.1:c.2345T>A	ENSP00000510161.1:p.Ile782Asn
ENST00000342694.7:c.2345T>A MANE Select	ENSP00000341083.2:p.Ile782Asn
ENST00000342694.6:c.2345T>A	ENSP00000341083.2:p.Ile782Asn
ENST00000421267.5:c.385T>A
ENST00000447210.5:c.122T>A	ENSP00000393029.1:p.Ile41Asn
ENST00000464810.5:n.2345T>A
NM_003995.3:c.2345T>A	NP_003986.2:p.Ile782Asn
XM_005251478.3:c.2354T>A	XP_005251535.1:p.Ile785Asn
XM_005251479.3:c.1367T>A	XP_005251536.1:p.Ile456Asn
XM_006716778.2:c.2282T>A	XP_006716841.1:p.Ile761Asn
XM_011517889.1:c.1367T>A	XP_011516191.1:p.Ile456Asn
XM_011517890.1:c.1367T>A	XP_011516192.1:p.Ile456Asn
XM_011517891.1:c.1367T>A	XP_011516193.1:p.Ile456Asn
XM_011517892.1:c.1367T>A	XP_011516194.1:p.Ile456Asn
XM_011517893.1:c.1367T>A	XP_011516195.1:p.Ile456Asn
XM_011517894.1:c.1367T>A	XP_011516196.1:p.Ile456Asn
XM_011517895.1:c.950T>A	XP_011516197.1:p.Ile317Asn
XM_024447556.1:c.2513T>A	XP_024303324.1:p.Ile838Asn
XM_024447557.1:c.2504T>A	XP_024303325.1:p.Ile835Asn
XM_024447558.1:c.1526T>A	XP_024303326.1:p.Ile509Asn
XM_024447559.1:c.1109T>A	XP_024303327.1:p.Ile370Asn
XM_024447560.1:c.1100T>A	XP_024303328.1:p.Ile367Asn
XM_024447561.1:c.941T>A	XP_024303329.1:p.Ile314Asn
NM_003995.4:c.2345T>A MANE Select	NP_003986.2:p.Ile782Asn
NM_001378923.1:c.2354T>A	NP_001365852.1:p.Ile785Asn