Canonical Allele Identifier: CA373379315

Gene: NPR2

Linked Data

• MyVariant Identifiers: chr9:g.35806195T>A (hg19) ; chr9:g.35806198T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35806198T>A , CM000671.2:g.35806198T>A	GRCh38
NC_000009.11:g.35806195T>A , CM000671.1:g.35806195T>A	GRCh37
NC_000009.10:g.35796195T>A	NCBI36
NG_009249.1:g.18790T>A
NG_047141.1:g.11075A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421267.6:c.377T>A
ENST00000448821.6:c.2337T>A	ENSP00000402902.2:p.Phe779Leu
ENST00000685871.1:c.2265T>A	ENSP00000509964.1:p.Phe755Leu
ENST00000686159.1:n.2376T>A
ENST00000686486.1:n.1507T>A
ENST00000687302.1:n.2451T>A
ENST00000687357.1:c.2190T>A	ENSP00000509549.1:p.Phe730Leu
ENST00000687625.1:n.1492T>A
ENST00000687787.1:c.2496T>A	ENSP00000509440.1:p.Phe832Leu
ENST00000688201.1:n.2294T>A
ENST00000688226.1:n.2269T>A
ENST00000688869.1:n.2643T>A
ENST00000689788.1:c.2131T>A	ENSP00000508973.1:n.2131T>A
ENST00000689898.1:c.2194T>A	ENSP00000509651.1:n.2194T>A
ENST00000690070.1:c.2421T>A	ENSP00000509654.1:p.Phe807Leu
ENST00000690267.1:c.2126T>A	ENSP00000510432.1:n.2126T>A
ENST00000690552.1:n.2198T>A
ENST00000691138.1:n.2126T>A
ENST00000691969.1:c.1837T>A	ENSP00000510244.1:n.1837T>A
ENST00000692232.1:n.3652T>A
ENST00000692233.1:c.2201T>A	ENSP00000509698.1:n.2201T>A
ENST00000692380.1:n.1492T>A
ENST00000692447.1:n.3453T>A
ENST00000693094.1:c.2337T>A	ENSP00000510161.1:p.Phe779Leu
ENST00000342694.7:c.2337T>A MANE Select	ENSP00000341083.2:p.Phe779Leu
ENST00000342694.6:c.2337T>A	ENSP00000341083.2:p.Phe779Leu
ENST00000421267.5:c.377T>A
ENST00000447210.5:c.114T>A	ENSP00000393029.1:p.Phe38Leu
ENST00000464810.5:n.2337T>A
NM_003995.3:c.2337T>A	NP_003986.2:p.Phe779Leu
XM_005251478.3:c.2346T>A	XP_005251535.1:p.Phe782Leu
XM_005251479.3:c.1359T>A	XP_005251536.1:p.Phe453Leu
XM_006716778.2:c.2274T>A	XP_006716841.1:p.Phe758Leu
XM_011517889.1:c.1359T>A	XP_011516191.1:p.Phe453Leu
XM_011517890.1:c.1359T>A	XP_011516192.1:p.Phe453Leu
XM_011517891.1:c.1359T>A	XP_011516193.1:p.Phe453Leu
XM_011517892.1:c.1359T>A	XP_011516194.1:p.Phe453Leu
XM_011517893.1:c.1359T>A	XP_011516195.1:p.Phe453Leu
XM_011517894.1:c.1359T>A	XP_011516196.1:p.Phe453Leu
XM_011517895.1:c.942T>A	XP_011516197.1:p.Phe314Leu
XM_024447556.1:c.2505T>A	XP_024303324.1:p.Phe835Leu
XM_024447557.1:c.2496T>A	XP_024303325.1:p.Phe832Leu
XM_024447558.1:c.1518T>A	XP_024303326.1:p.Phe506Leu
XM_024447559.1:c.1101T>A	XP_024303327.1:p.Phe367Leu
XM_024447560.1:c.1092T>A	XP_024303328.1:p.Phe364Leu
XM_024447561.1:c.933T>A	XP_024303329.1:p.Phe311Leu
NM_003995.4:c.2337T>A MANE Select	NP_003986.2:p.Phe779Leu
NM_001378923.1:c.2346T>A	NP_001365852.1:p.Phe782Leu