Canonical Allele Identifier: CA373379021

Gene: NPR2

Linked Data

• MyVariant Identifiers: chr9:g.35806139C>G (hg19) ; chr9:g.35806142C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35806142C>G , CM000671.2:g.35806142C>G	GRCh38
NC_000009.11:g.35806139C>G , CM000671.1:g.35806139C>G	GRCh37
NC_000009.10:g.35796139C>G	NCBI36
NG_009249.1:g.18734C>G
NG_047141.1:g.11131G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421267.6:c.321C>G
ENST00000448821.6:c.2281C>G	ENSP00000402902.2:p.Leu761Val
ENST00000685871.1:c.2209C>G	ENSP00000509964.1:p.Leu737Val
ENST00000686159.1:n.2320C>G
ENST00000686486.1:n.1451C>G
ENST00000687302.1:n.2395C>G
ENST00000687357.1:c.2134C>G	ENSP00000509549.1:p.Leu712Val
ENST00000687625.1:n.1436C>G
ENST00000687787.1:c.2440C>G	ENSP00000509440.1:p.Leu814Val
ENST00000688201.1:n.2238C>G
ENST00000688226.1:n.2213C>G
ENST00000688869.1:n.2587C>G
ENST00000689788.1:c.2075C>G	ENSP00000508973.1:n.2075C>G
ENST00000689898.1:c.2138C>G	ENSP00000509651.1:n.2138C>G
ENST00000690070.1:c.2365C>G	ENSP00000509654.1:p.Leu789Val
ENST00000690267.1:c.2070C>G	ENSP00000510432.1:n.2070C>G
ENST00000690552.1:n.2142C>G
ENST00000691138.1:n.2070C>G
ENST00000691969.1:c.1781C>G	ENSP00000510244.1:n.1781C>G
ENST00000692232.1:n.3596C>G
ENST00000692233.1:c.2145C>G	ENSP00000509698.1:n.2145C>G
ENST00000692380.1:n.1436C>G
ENST00000692447.1:n.3397C>G
ENST00000693094.1:c.2281C>G	ENSP00000510161.1:p.Leu761Val
ENST00000342694.7:c.2281C>G MANE Select	ENSP00000341083.2:p.Leu761Val
ENST00000342694.6:c.2281C>G	ENSP00000341083.2:p.Leu761Val
ENST00000421267.5:c.321C>G
ENST00000447210.5:c.58C>G	ENSP00000393029.1:p.Leu20Val
ENST00000464810.5:n.2281C>G
NM_003995.3:c.2281C>G	NP_003986.2:p.Leu761Val
XM_005251478.3:c.2290C>G	XP_005251535.1:p.Leu764Val
XM_005251479.3:c.1303C>G	XP_005251536.1:p.Leu435Val
XM_006716778.2:c.2218C>G	XP_006716841.1:p.Leu740Val
XM_011517889.1:c.1303C>G	XP_011516191.1:p.Leu435Val
XM_011517890.1:c.1303C>G	XP_011516192.1:p.Leu435Val
XM_011517891.1:c.1303C>G	XP_011516193.1:p.Leu435Val
XM_011517892.1:c.1303C>G	XP_011516194.1:p.Leu435Val
XM_011517893.1:c.1303C>G	XP_011516195.1:p.Leu435Val
XM_011517894.1:c.1303C>G	XP_011516196.1:p.Leu435Val
XM_011517895.1:c.886C>G	XP_011516197.1:p.Leu296Val
XM_024447556.1:c.2449C>G	XP_024303324.1:p.Leu817Val
XM_024447557.1:c.2440C>G	XP_024303325.1:p.Leu814Val
XM_024447558.1:c.1462C>G	XP_024303326.1:p.Leu488Val
XM_024447559.1:c.1045C>G	XP_024303327.1:p.Leu349Val
XM_024447560.1:c.1036C>G	XP_024303328.1:p.Leu346Val
XM_024447561.1:c.877C>G	XP_024303329.1:p.Leu293Val
NM_003995.4:c.2281C>G MANE Select	NP_003986.2:p.Leu761Val
NM_001378923.1:c.2290C>G	NP_001365852.1:p.Leu764Val