Canonical Allele Identifier: CA1846133491
Gene: NPR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.35801091T= , CM000671.2:g.35801091T= GRCh38
NC_000009.11:g.35801088T= , CM000671.1:g.35801088T= GRCh37
NC_000009.10:g.35791088T= NCBI36
NG_009249.1:g.13683T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000448821.6:c.1373T= ENSP00000402902.2:p.Ile458=
ENST00000685871.1:c.1373T= ENSP00000509964.1:p.Ile458=
ENST00000686159.1:n.1412T=
ENST00000686486.1:n.381T=
ENST00000687302.1:n.1459T=
ENST00000687357.1:c.1373T= ENSP00000509549.1:p.Ile458=
ENST00000687625.1:n.528T=
ENST00000687787.1:c.1373T= ENSP00000509440.1:p.Ile458=
ENST00000688201.1:n.1405T=
ENST00000688226.1:n.1305T=
ENST00000688869.1:n.1679T=
ENST00000689788.1:c.1167T= ENSP00000508973.1:n.1167T=
ENST00000689898.1:c.1377T= ENSP00000509651.1:p.Asn459=
ENST00000690070.1:c.1373T= ENSP00000509654.1:p.Ile458=
ENST00000690267.1:c.1237T= ENSP00000510432.1:n.1237T=
ENST00000690552.1:n.1234T=
ENST00000691138.1:n.1234T=
ENST00000691969.1:c.948T= ENSP00000510244.1:n.948T=
ENST00000692232.1:n.2529T=
ENST00000692233.1:c.1237T= ENSP00000509698.1:n.1237T=
ENST00000692380.1:n.528T=
ENST00000692447.1:n.2489T=
ENST00000693094.1:c.1373T= ENSP00000510161.1:p.Ile458=
ENST00000342694.7:c.1373T= MANE Select ENSP00000341083.2:p.Ile458=
ENST00000342694.6:c.1373T= ENSP00000341083.2:p.Ile458=
ENST00000464810.5:n.1373T=
NM_003995.3:c.1373T= NP_003986.2:p.Ile458=
XM_005251478.3:c.1373T= XP_005251535.1:p.Ile458=
XM_005251479.3:c.386T= XP_005251536.1:p.Ile129=
XM_006716778.2:c.1373T= XP_006716841.1:p.Ile458=
XM_011517889.1:c.386T= XP_011516191.1:p.Ile129=
XM_011517890.1:c.386T= XP_011516192.1:p.Ile129=
XM_011517891.1:c.386T= XP_011516193.1:p.Ile129=
XM_011517892.1:c.386T= XP_011516194.1:p.Ile129=
XM_011517893.1:c.386T= XP_011516195.1:p.Ile129=
XM_011517894.1:c.386T= XP_011516196.1:p.Ile129=
XM_011517895.1:c.-32T= XP_011516197.1:n.-32T=
XM_024447556.1:c.1373T= XP_024303324.1:p.Ile458=
XM_024447557.1:c.1373T= XP_024303325.1:p.Ile458=
XM_024447558.1:c.386T= XP_024303326.1:p.Ile129=
XM_024447559.1:c.-32T= XP_024303327.1:n.-32T=
XM_024447560.1:c.-32T= XP_024303328.1:n.-32T=
XM_024447561.1:c.-32T= XP_024303329.1:n.-32T=
NM_003995.4:c.1373T= MANE Select NP_003986.2:p.Ile458=
NM_001378923.1:c.1373T= NP_001365852.1:p.Ile458=