Canonical Allele Identifier: CA1846146210
Gene: NPR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.35806172C= , CM000671.2:g.35806172C= GRCh38
NC_000009.11:g.35806169C= , CM000671.1:g.35806169C= GRCh37
NC_000009.10:g.35796169C= NCBI36
NG_009249.1:g.18764C=
NG_047141.1:g.11101G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000421267.6:c.351C=
ENST00000448821.6:c.2311C= ENSP00000402902.2:p.Gln771=
ENST00000685871.1:c.2239C= ENSP00000509964.1:p.Gln747=
ENST00000686159.1:n.2350C=
ENST00000686486.1:n.1481C=
ENST00000687302.1:n.2425C=
ENST00000687357.1:c.2164C= ENSP00000509549.1:p.Gln722=
ENST00000687625.1:n.1466C=
ENST00000687787.1:c.2470C= ENSP00000509440.1:p.Gln824=
ENST00000688201.1:n.2268C=
ENST00000688226.1:n.2243C=
ENST00000688869.1:n.2617C=
ENST00000689788.1:c.2105C= ENSP00000508973.1:n.2105C=
ENST00000689898.1:c.2168C= ENSP00000509651.1:n.2168C=
ENST00000690070.1:c.2395C= ENSP00000509654.1:p.Gln799=
ENST00000690267.1:c.2100C= ENSP00000510432.1:n.2100C=
ENST00000690552.1:n.2172C=
ENST00000691138.1:n.2100C=
ENST00000691969.1:c.1811C= ENSP00000510244.1:n.1811C=
ENST00000692232.1:n.3626C=
ENST00000692233.1:c.2175C= ENSP00000509698.1:n.2175C=
ENST00000692380.1:n.1466C=
ENST00000692447.1:n.3427C=
ENST00000693094.1:c.2311C= ENSP00000510161.1:p.Gln771=
ENST00000342694.7:c.2311C= MANE Select ENSP00000341083.2:p.Gln771=
ENST00000342694.6:c.2311C= ENSP00000341083.2:p.Gln771=
ENST00000421267.5:c.351C=
ENST00000447210.5:c.88C= ENSP00000393029.1:p.Gln30=
ENST00000464810.5:n.2311C=
NM_003995.3:c.2311C= NP_003986.2:p.Gln771=
XM_005251478.3:c.2320C= XP_005251535.1:p.Gln774=
XM_005251479.3:c.1333C= XP_005251536.1:p.Gln445=
XM_006716778.2:c.2248C= XP_006716841.1:p.Gln750=
XM_011517889.1:c.1333C= XP_011516191.1:p.Gln445=
XM_011517890.1:c.1333C= XP_011516192.1:p.Gln445=
XM_011517891.1:c.1333C= XP_011516193.1:p.Gln445=
XM_011517892.1:c.1333C= XP_011516194.1:p.Gln445=
XM_011517893.1:c.1333C= XP_011516195.1:p.Gln445=
XM_011517894.1:c.1333C= XP_011516196.1:p.Gln445=
XM_011517895.1:c.916C= XP_011516197.1:p.Gln306=
XM_024447556.1:c.2479C= XP_024303324.1:p.Gln827=
XM_024447557.1:c.2470C= XP_024303325.1:p.Gln824=
XM_024447558.1:c.1492C= XP_024303326.1:p.Gln498=
XM_024447559.1:c.1075C= XP_024303327.1:p.Gln359=
XM_024447560.1:c.1066C= XP_024303328.1:p.Gln356=
XM_024447561.1:c.907C= XP_024303329.1:p.Gln303=
NM_003995.4:c.2311C= MANE Select NP_003986.2:p.Gln771=
NM_001378923.1:c.2320C= NP_001365852.1:p.Gln774=