Canonical Allele Identifier: CA373379421

Gene: NPR2

Linked Data

• MyVariant Identifiers: chr9:g.35806214A>G (hg19) ; chr9:g.35806217A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35806217A>G , CM000671.2:g.35806217A>G	GRCh38
NC_000009.11:g.35806214A>G , CM000671.1:g.35806214A>G	GRCh37
NC_000009.10:g.35796214A>G	NCBI36
NG_009249.1:g.18809A>G
NG_047141.1:g.11056T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421267.6:c.396A>G
ENST00000448821.6:c.2356A>G	ENSP00000402902.2:p.Ile786Val
ENST00000685871.1:c.2284A>G	ENSP00000509964.1:p.Ile762Val
ENST00000686159.1:n.2395A>G
ENST00000686486.1:n.1526A>G
ENST00000687302.1:n.2470A>G
ENST00000687357.1:c.2209A>G	ENSP00000509549.1:p.Ile737Val
ENST00000687625.1:n.1511A>G
ENST00000687787.1:c.2515A>G	ENSP00000509440.1:p.Ile839Val
ENST00000688201.1:n.2313A>G
ENST00000688226.1:n.2288A>G
ENST00000688869.1:n.2662A>G
ENST00000689788.1:c.2150A>G	ENSP00000508973.1:n.2150A>G
ENST00000689898.1:c.2213A>G	ENSP00000509651.1:n.2213A>G
ENST00000690070.1:c.2440A>G	ENSP00000509654.1:p.Ile814Val
ENST00000690267.1:c.2145A>G	ENSP00000510432.1:n.2145A>G
ENST00000690552.1:n.2217A>G
ENST00000691138.1:n.2145A>G
ENST00000691969.1:c.1856A>G	ENSP00000510244.1:n.1856A>G
ENST00000692232.1:n.3671A>G
ENST00000692233.1:c.2220A>G	ENSP00000509698.1:n.2220A>G
ENST00000692380.1:n.1511A>G
ENST00000692447.1:n.3472A>G
ENST00000693094.1:c.2356A>G	ENSP00000510161.1:p.Ile786Val
ENST00000342694.7:c.2356A>G MANE Select	ENSP00000341083.2:p.Ile786Val
ENST00000342694.6:c.2356A>G	ENSP00000341083.2:p.Ile786Val
ENST00000421267.5:c.396A>G
ENST00000447210.5:c.133A>G	ENSP00000393029.1:p.Ile45Val
ENST00000464810.5:n.2356A>G
NM_003995.3:c.2356A>G	NP_003986.2:p.Ile786Val
XM_005251478.3:c.2365A>G	XP_005251535.1:p.Ile789Val
XM_005251479.3:c.1378A>G	XP_005251536.1:p.Ile460Val
XM_006716778.2:c.2293A>G	XP_006716841.1:p.Ile765Val
XM_011517889.1:c.1378A>G	XP_011516191.1:p.Ile460Val
XM_011517890.1:c.1378A>G	XP_011516192.1:p.Ile460Val
XM_011517891.1:c.1378A>G	XP_011516193.1:p.Ile460Val
XM_011517892.1:c.1378A>G	XP_011516194.1:p.Ile460Val
XM_011517893.1:c.1378A>G	XP_011516195.1:p.Ile460Val
XM_011517894.1:c.1378A>G	XP_011516196.1:p.Ile460Val
XM_011517895.1:c.961A>G	XP_011516197.1:p.Ile321Val
XM_024447556.1:c.2524A>G	XP_024303324.1:p.Ile842Val
XM_024447557.1:c.2515A>G	XP_024303325.1:p.Ile839Val
XM_024447558.1:c.1537A>G	XP_024303326.1:p.Ile513Val
XM_024447559.1:c.1120A>G	XP_024303327.1:p.Ile374Val
XM_024447560.1:c.1111A>G	XP_024303328.1:p.Ile371Val
XM_024447561.1:c.952A>G	XP_024303329.1:p.Ile318Val
NM_003995.4:c.2356A>G MANE Select	NP_003986.2:p.Ile786Val
NM_001378923.1:c.2365A>G	NP_001365852.1:p.Ile789Val