Canonical Allele Identifier: CA373378734

Gene: NPR2

Linked Data

• MyVariant Identifiers: chr9:g.35806072G>T (hg19) ; chr9:g.35806075G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35806075G>T , CM000671.2:g.35806075G>T	GRCh38
NC_000009.11:g.35806072G>T , CM000671.1:g.35806072G>T	GRCh37
NC_000009.10:g.35796072G>T	NCBI36
NG_009249.1:g.18667G>T
NG_047141.1:g.11198C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421267.6:c.254G>T
ENST00000448821.6:c.2214G>T	ENSP00000402902.2:p.Gln738His
ENST00000685871.1:c.2142G>T	ENSP00000509964.1:p.Gln714His
ENST00000686159.1:n.2253G>T
ENST00000686486.1:n.1384G>T
ENST00000687302.1:n.2328G>T
ENST00000687357.1:c.2067G>T	ENSP00000509549.1:p.Gln689His
ENST00000687625.1:n.1369G>T
ENST00000687787.1:c.2373G>T	ENSP00000509440.1:p.Gln791His
ENST00000688201.1:n.2171G>T
ENST00000688226.1:n.2146G>T
ENST00000688869.1:n.2520G>T
ENST00000689788.1:c.2008G>T	ENSP00000508973.1:n.2008G>T
ENST00000689898.1:c.2071G>T	ENSP00000509651.1:n.2071G>T
ENST00000690070.1:c.2298G>T	ENSP00000509654.1:p.Gln766His
ENST00000690267.1:c.2003G>T	ENSP00000510432.1:n.2003G>T
ENST00000690552.1:n.2075G>T
ENST00000691138.1:n.2003G>T
ENST00000691969.1:c.1714G>T	ENSP00000510244.1:n.1714G>T
ENST00000692232.1:n.3529G>T
ENST00000692233.1:c.2078G>T	ENSP00000509698.1:n.2078G>T
ENST00000692380.1:n.1369G>T
ENST00000692447.1:n.3330G>T
ENST00000693094.1:c.2214G>T	ENSP00000510161.1:p.Gln738His
ENST00000342694.7:c.2214G>T MANE Select	ENSP00000341083.2:p.Gln738His
ENST00000342694.6:c.2214G>T	ENSP00000341083.2:p.Gln738His
ENST00000421267.5:c.254G>T
ENST00000464810.5:n.2214G>T
NM_003995.3:c.2214G>T	NP_003986.2:p.Gln738His
XM_005251478.3:c.2223G>T	XP_005251535.1:p.Gln741His
XM_005251479.3:c.1236G>T	XP_005251536.1:p.Gln412His
XM_006716778.2:c.2151G>T	XP_006716841.1:p.Gln717His
XM_011517889.1:c.1236G>T	XP_011516191.1:p.Gln412His
XM_011517890.1:c.1236G>T	XP_011516192.1:p.Gln412His
XM_011517891.1:c.1236G>T	XP_011516193.1:p.Gln412His
XM_011517892.1:c.1236G>T	XP_011516194.1:p.Gln412His
XM_011517893.1:c.1236G>T	XP_011516195.1:p.Gln412His
XM_011517894.1:c.1236G>T	XP_011516196.1:p.Gln412His
XM_011517895.1:c.819G>T	XP_011516197.1:p.Gln273His
XM_024447556.1:c.2382G>T	XP_024303324.1:p.Gln794His
XM_024447557.1:c.2373G>T	XP_024303325.1:p.Gln791His
XM_024447558.1:c.1395G>T	XP_024303326.1:p.Gln465His
XM_024447559.1:c.978G>T	XP_024303327.1:p.Gln326His
XM_024447560.1:c.969G>T	XP_024303328.1:p.Gln323His
XM_024447561.1:c.810G>T	XP_024303329.1:p.Gln270His
NM_003995.4:c.2214G>T MANE Select	NP_003986.2:p.Gln738His
NM_001378923.1:c.2223G>T	NP_001365852.1:p.Gln741His