Canonical Allele Identifier: CA373379029

Gene: NPR2

Linked Data

• MyVariant Identifiers: chr9:g.35806140T>G (hg19) ; chr9:g.35806143T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35806143T>G , CM000671.2:g.35806143T>G	GRCh38
NC_000009.11:g.35806140T>G , CM000671.1:g.35806140T>G	GRCh37
NC_000009.10:g.35796140T>G	NCBI36
NG_009249.1:g.18735T>G
NG_047141.1:g.11130A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421267.6:c.322T>G
ENST00000448821.6:c.2282T>G	ENSP00000402902.2:p.Leu761Arg
ENST00000685871.1:c.2210T>G	ENSP00000509964.1:p.Leu737Arg
ENST00000686159.1:n.2321T>G
ENST00000686486.1:n.1452T>G
ENST00000687302.1:n.2396T>G
ENST00000687357.1:c.2135T>G	ENSP00000509549.1:p.Leu712Arg
ENST00000687625.1:n.1437T>G
ENST00000687787.1:c.2441T>G	ENSP00000509440.1:p.Leu814Arg
ENST00000688201.1:n.2239T>G
ENST00000688226.1:n.2214T>G
ENST00000688869.1:n.2588T>G
ENST00000689788.1:c.2076T>G	ENSP00000508973.1:n.2076T>G
ENST00000689898.1:c.2139T>G	ENSP00000509651.1:n.2139T>G
ENST00000690070.1:c.2366T>G	ENSP00000509654.1:p.Leu789Arg
ENST00000690267.1:c.2071T>G	ENSP00000510432.1:n.2071T>G
ENST00000690552.1:n.2143T>G
ENST00000691138.1:n.2071T>G
ENST00000691969.1:c.1782T>G	ENSP00000510244.1:n.1782T>G
ENST00000692232.1:n.3597T>G
ENST00000692233.1:c.2146T>G	ENSP00000509698.1:n.2146T>G
ENST00000692380.1:n.1437T>G
ENST00000692447.1:n.3398T>G
ENST00000693094.1:c.2282T>G	ENSP00000510161.1:p.Leu761Arg
ENST00000342694.7:c.2282T>G MANE Select	ENSP00000341083.2:p.Leu761Arg
ENST00000342694.6:c.2282T>G	ENSP00000341083.2:p.Leu761Arg
ENST00000421267.5:c.322T>G
ENST00000447210.5:c.59T>G	ENSP00000393029.1:p.Leu20Arg
ENST00000464810.5:n.2282T>G
NM_003995.3:c.2282T>G	NP_003986.2:p.Leu761Arg
XM_005251478.3:c.2291T>G	XP_005251535.1:p.Leu764Arg
XM_005251479.3:c.1304T>G	XP_005251536.1:p.Leu435Arg
XM_006716778.2:c.2219T>G	XP_006716841.1:p.Leu740Arg
XM_011517889.1:c.1304T>G	XP_011516191.1:p.Leu435Arg
XM_011517890.1:c.1304T>G	XP_011516192.1:p.Leu435Arg
XM_011517891.1:c.1304T>G	XP_011516193.1:p.Leu435Arg
XM_011517892.1:c.1304T>G	XP_011516194.1:p.Leu435Arg
XM_011517893.1:c.1304T>G	XP_011516195.1:p.Leu435Arg
XM_011517894.1:c.1304T>G	XP_011516196.1:p.Leu435Arg
XM_011517895.1:c.887T>G	XP_011516197.1:p.Leu296Arg
XM_024447556.1:c.2450T>G	XP_024303324.1:p.Leu817Arg
XM_024447557.1:c.2441T>G	XP_024303325.1:p.Leu814Arg
XM_024447558.1:c.1463T>G	XP_024303326.1:p.Leu488Arg
XM_024447559.1:c.1046T>G	XP_024303327.1:p.Leu349Arg
XM_024447560.1:c.1037T>G	XP_024303328.1:p.Leu346Arg
XM_024447561.1:c.878T>G	XP_024303329.1:p.Leu293Arg
NM_003995.4:c.2282T>G MANE Select	NP_003986.2:p.Leu761Arg
NM_001378923.1:c.2291T>G	NP_001365852.1:p.Leu764Arg