Canonical Allele Identifier: CA1846183949
Gene: NPR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.35792314C= , CM000671.2:g.35792314C= GRCh38
NC_000009.11:g.35792311C= , CM000671.1:g.35792311C= GRCh37
NC_000009.10:g.35782311C= NCBI36
NG_009249.1:g.4906C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000686159.1:n.74-129C=
ENST00000687625.1:n.164+1148C=
ENST00000688201.1:n.67-129C=
ENST00000692380.1:n.164+1148C=
ENST00000342694.7:c.-95C= MANE Select ENSP00000341083.2:n.-95C=
ENST00000342694.6:c.-95C= ENSP00000341083.2:n.-95C=
XM_005251478.3:c.-95C= XP_005251535.1:n.-95C=
XM_005251479.3:c.-115+1974C= XP_005251536.1:n.-115+1974C=
XM_006716778.2:c.-95C= XP_006716841.1:n.-95C=
XM_011517889.1:c.-115+1974C= XP_011516191.1:n.-115+1974C=
XM_011517890.1:c.-115+1974C= XP_011516192.1:n.-115+1974C=
XM_011517891.1:c.-115+1974C= XP_011516193.1:n.-115+1974C=
XM_011517892.1:c.-115+1974C= XP_011516194.1:n.-115+1974C=
XM_011517893.1:c.-115+1974C= XP_011516195.1:n.-115+1974C=
XM_011517894.1:c.-115+1974C= XP_011516196.1:n.-115+1974C=
XM_024447556.1:c.-95C= XP_024303324.1:n.-95C=
XM_024447557.1:c.-95C= XP_024303325.1:n.-95C=
XM_024447558.1:c.-115+1974C= XP_024303326.1:n.-115+1974C=
NM_003995.4:c.-95C= MANE Select NP_003986.2:n.-95C=
NM_001378923.1:c.-95C= NP_001365852.1:n.-95C=