Canonical Allele Identifier: CA373379440

Gene: NPR2

Linked Data

• MyVariant Identifiers: chr9:g.35806223T>A (hg19) ; chr9:g.35806226T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35806226T>A , CM000671.2:g.35806226T>A	GRCh38
NC_000009.11:g.35806223T>A , CM000671.1:g.35806223T>A	GRCh37
NC_000009.10:g.35796223T>A	NCBI36
NG_009249.1:g.18818T>A
NG_047141.1:g.11047A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421267.6:c.405T>A
ENST00000448821.6:c.2365T>A	ENSP00000402902.2:p.Phe789Ile
ENST00000685871.1:c.2293T>A	ENSP00000509964.1:p.Phe765Ile
ENST00000686159.1:n.2404T>A
ENST00000686486.1:n.1535T>A
ENST00000687302.1:n.2479T>A
ENST00000687357.1:c.2218T>A	ENSP00000509549.1:p.Phe740Ile
ENST00000687625.1:n.1520T>A
ENST00000687787.1:c.2524T>A	ENSP00000509440.1:p.Phe842Ile
ENST00000688201.1:n.2322T>A
ENST00000688226.1:n.2297T>A
ENST00000688869.1:n.2671T>A
ENST00000689788.1:c.2159T>A	ENSP00000508973.1:n.2159T>A
ENST00000689898.1:c.2222T>A	ENSP00000509651.1:n.2222T>A
ENST00000690070.1:c.2449T>A	ENSP00000509654.1:p.Phe817Ile
ENST00000690267.1:c.2154T>A	ENSP00000510432.1:n.2154T>A
ENST00000690552.1:n.2226T>A
ENST00000691138.1:n.2154T>A
ENST00000691969.1:c.1865T>A	ENSP00000510244.1:n.1865T>A
ENST00000692232.1:n.3680T>A
ENST00000692233.1:c.2229T>A	ENSP00000509698.1:n.2229T>A
ENST00000692380.1:n.1520T>A
ENST00000692447.1:n.3481T>A
ENST00000693094.1:c.2365T>A	ENSP00000510161.1:p.Phe789Ile
ENST00000342694.7:c.2365T>A MANE Select	ENSP00000341083.2:p.Phe789Ile
ENST00000342694.6:c.2365T>A	ENSP00000341083.2:p.Phe789Ile
ENST00000421267.5:c.405T>A
ENST00000447210.5:c.142T>A	ENSP00000393029.1:p.Phe48Ile
ENST00000464810.5:n.2365T>A
NM_003995.3:c.2365T>A	NP_003986.2:p.Phe789Ile
XM_005251478.3:c.2374T>A	XP_005251535.1:p.Phe792Ile
XM_005251479.3:c.1387T>A	XP_005251536.1:p.Phe463Ile
XM_006716778.2:c.2302T>A	XP_006716841.1:p.Phe768Ile
XM_011517889.1:c.1387T>A	XP_011516191.1:p.Phe463Ile
XM_011517890.1:c.1387T>A	XP_011516192.1:p.Phe463Ile
XM_011517891.1:c.1387T>A	XP_011516193.1:p.Phe463Ile
XM_011517892.1:c.1387T>A	XP_011516194.1:p.Phe463Ile
XM_011517893.1:c.1387T>A	XP_011516195.1:p.Phe463Ile
XM_011517894.1:c.1387T>A	XP_011516196.1:p.Phe463Ile
XM_011517895.1:c.970T>A	XP_011516197.1:p.Phe324Ile
XM_024447556.1:c.2533T>A	XP_024303324.1:p.Phe845Ile
XM_024447557.1:c.2524T>A	XP_024303325.1:p.Phe842Ile
XM_024447558.1:c.1546T>A	XP_024303326.1:p.Phe516Ile
XM_024447559.1:c.1129T>A	XP_024303327.1:p.Phe377Ile
XM_024447560.1:c.1120T>A	XP_024303328.1:p.Phe374Ile
XM_024447561.1:c.961T>A	XP_024303329.1:p.Phe321Ile
NM_003995.4:c.2365T>A MANE Select	NP_003986.2:p.Phe789Ile
NM_001378923.1:c.2374T>A	NP_001365852.1:p.Phe792Ile