Canonical Allele Identifier: CA373379782

Gene: NPR2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35806443T>G , CM000671.2:g.35806443T>G	GRCh38
NC_000009.11:g.35806440T>G , CM000671.1:g.35806440T>G	GRCh37
NC_000009.10:g.35796440T>G	NCBI36
NG_009249.1:g.19035T>G
NG_047141.1:g.10830A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_003995.4:c.2424T>G MANE Select	NP_003986.2:p.Tyr808Ter
ENST00000342694.7:c.2424T>G MANE Select	ENSP00000341083.2:p.Tyr808Ter
NM_001378923.1:c.2433T>G	NP_001365852.1:p.Tyr811Ter
NM_003995.3:c.2424T>G	NP_003986.2:p.Tyr808Ter
ENST00000342694.6:c.2424T>G	ENSP00000341083.2:p.Tyr808Ter
ENST00000421267.5:c.464T>G
ENST00000421267.6:c.464T>G
ENST00000447210.5:c.201T>G	ENSP00000393029.1:p.Tyr67Ter
ENST00000448821.6:c.2424T>G	ENSP00000402902.2:p.Tyr808Ter
ENST00000464810.5:n.2424T>G
ENST00000685871.1:c.2352T>G	ENSP00000509964.1:p.Tyr784Ter
ENST00000686159.1:n.2463T>G
ENST00000686486.1:n.1594T>G
ENST00000687302.1:n.2538T>G
ENST00000687357.1:c.2277T>G	ENSP00000509549.1:p.Tyr759Ter
ENST00000687625.1:n.1579T>G
ENST00000687787.1:c.2583T>G	ENSP00000509440.1:p.Tyr861Ter
ENST00000688201.1:n.2381T>G
ENST00000688226.1:n.2356T>G
ENST00000688869.1:n.2730T>G
ENST00000689788.1:c.2218T>G	ENSP00000508973.1:n.2218T>G
ENST00000689898.1:c.2281T>G	ENSP00000509651.1:n.2281T>G
ENST00000690070.1:c.2508T>G	ENSP00000509654.1:p.Tyr836Ter
ENST00000690267.1:c.2213T>G	ENSP00000510432.1:n.2213T>G
ENST00000690552.1:n.2285T>G
ENST00000691138.1:n.2213T>G
ENST00000691969.1:c.1924T>G	ENSP00000510244.1:n.1924T>G
ENST00000692232.1:n.3739T>G
ENST00000692233.1:c.2288T>G	ENSP00000509698.1:n.2288T>G
ENST00000692380.1:n.1579T>G
ENST00000692447.1:n.3540T>G
ENST00000693094.1:c.2424T>G	ENSP00000510161.1:p.Tyr808Ter
XM_005251478.3:c.2433T>G	XP_005251535.1:p.Tyr811Ter
XM_005251479.3:c.1446T>G	XP_005251536.1:p.Tyr482Ter
XM_006716778.2:c.2361T>G	XP_006716841.1:p.Tyr787Ter
XM_011517889.1:c.1446T>G	XP_011516191.1:p.Tyr482Ter
XM_011517890.1:c.1446T>G	XP_011516192.1:p.Tyr482Ter
XM_011517891.1:c.1446T>G	XP_011516193.1:p.Tyr482Ter
XM_011517892.1:c.1446T>G	XP_011516194.1:p.Tyr482Ter
XM_011517893.1:c.1446T>G	XP_011516195.1:p.Tyr482Ter
XM_011517894.1:c.1446T>G	XP_011516196.1:p.Tyr482Ter
XM_011517895.1:c.1029T>G	XP_011516197.1:p.Tyr343Ter
XM_024447556.1:c.2592T>G	XP_024303324.1:p.Tyr864Ter
XM_024447557.1:c.2583T>G	XP_024303325.1:p.Tyr861Ter
XM_024447558.1:c.1605T>G	XP_024303326.1:p.Tyr535Ter
XM_024447559.1:c.1188T>G	XP_024303327.1:p.Tyr396Ter
XM_024447560.1:c.1179T>G	XP_024303328.1:p.Tyr393Ter
XM_024447561.1:c.1020T>G	XP_024303329.1:p.Tyr340Ter