Canonical Allele Identifier: CA373379088

Gene: NPR2

Linked Data

• MyVariant Identifiers: chr9:g.35806151A>T (hg19) ; chr9:g.35806154A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35806154A>T , CM000671.2:g.35806154A>T	GRCh38
NC_000009.11:g.35806151A>T , CM000671.1:g.35806151A>T	GRCh37
NC_000009.10:g.35796151A>T	NCBI36
NG_009249.1:g.18746A>T
NG_047141.1:g.11119T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421267.6:c.333A>T
ENST00000448821.6:c.2293A>T	ENSP00000402902.2:p.Met765Leu
ENST00000685871.1:c.2221A>T	ENSP00000509964.1:p.Met741Leu
ENST00000686159.1:n.2332A>T
ENST00000686486.1:n.1463A>T
ENST00000687302.1:n.2407A>T
ENST00000687357.1:c.2146A>T	ENSP00000509549.1:p.Met716Leu
ENST00000687625.1:n.1448A>T
ENST00000687787.1:c.2452A>T	ENSP00000509440.1:p.Met818Leu
ENST00000688201.1:n.2250A>T
ENST00000688226.1:n.2225A>T
ENST00000688869.1:n.2599A>T
ENST00000689788.1:c.2087A>T	ENSP00000508973.1:n.2087A>T
ENST00000689898.1:c.2150A>T	ENSP00000509651.1:n.2150A>T
ENST00000690070.1:c.2377A>T	ENSP00000509654.1:p.Met793Leu
ENST00000690267.1:c.2082A>T	ENSP00000510432.1:n.2082A>T
ENST00000690552.1:n.2154A>T
ENST00000691138.1:n.2082A>T
ENST00000691969.1:c.1793A>T	ENSP00000510244.1:n.1793A>T
ENST00000692232.1:n.3608A>T
ENST00000692233.1:c.2157A>T	ENSP00000509698.1:n.2157A>T
ENST00000692380.1:n.1448A>T
ENST00000692447.1:n.3409A>T
ENST00000693094.1:c.2293A>T	ENSP00000510161.1:p.Met765Leu
ENST00000342694.7:c.2293A>T MANE Select	ENSP00000341083.2:p.Met765Leu
ENST00000342694.6:c.2293A>T	ENSP00000341083.2:p.Met765Leu
ENST00000421267.5:c.333A>T
ENST00000447210.5:c.70A>T	ENSP00000393029.1:p.Met24Leu
ENST00000464810.5:n.2293A>T
NM_003995.3:c.2293A>T	NP_003986.2:p.Met765Leu
XM_005251478.3:c.2302A>T	XP_005251535.1:p.Met768Leu
XM_005251479.3:c.1315A>T	XP_005251536.1:p.Met439Leu
XM_006716778.2:c.2230A>T	XP_006716841.1:p.Met744Leu
XM_011517889.1:c.1315A>T	XP_011516191.1:p.Met439Leu
XM_011517890.1:c.1315A>T	XP_011516192.1:p.Met439Leu
XM_011517891.1:c.1315A>T	XP_011516193.1:p.Met439Leu
XM_011517892.1:c.1315A>T	XP_011516194.1:p.Met439Leu
XM_011517893.1:c.1315A>T	XP_011516195.1:p.Met439Leu
XM_011517894.1:c.1315A>T	XP_011516196.1:p.Met439Leu
XM_011517895.1:c.898A>T	XP_011516197.1:p.Met300Leu
XM_024447556.1:c.2461A>T	XP_024303324.1:p.Met821Leu
XM_024447557.1:c.2452A>T	XP_024303325.1:p.Met818Leu
XM_024447558.1:c.1474A>T	XP_024303326.1:p.Met492Leu
XM_024447559.1:c.1057A>T	XP_024303327.1:p.Met353Leu
XM_024447560.1:c.1048A>T	XP_024303328.1:p.Met350Leu
XM_024447561.1:c.889A>T	XP_024303329.1:p.Met297Leu
NM_003995.4:c.2293A>T MANE Select	NP_003986.2:p.Met765Leu
NM_001378923.1:c.2302A>T	NP_001365852.1:p.Met768Leu