Canonical Allele Identifier: CA2689909798

Gene: NPR2

Linked Data

• gnomAD v4: 9-35792404-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35792404T>C , CM000671.2:g.35792404T>C	GRCh38
NC_000009.11:g.35792401T>C , CM000671.1:g.35792401T>C	GRCh37
NC_000009.10:g.35782401T>C	NCBI36
NG_009249.1:g.4996T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000685871.1:c.-5T>C	ENSP00000509964.1:n.-5T>C
ENST00000686159.1:n.74-39T>C
ENST00000687625.1:n.164+1238T>C
ENST00000688201.1:n.67-39T>C
ENST00000688869.1:n.77T>C
ENST00000692380.1:n.164+1238T>C
ENST00000342694.7:c.-5T>C MANE Select	ENSP00000341083.2:n.-5T>C
ENST00000342694.6:c.-5T>C	ENSP00000341083.2:n.-5T>C
XM_005251478.3:c.-5T>C	XP_005251535.1:n.-5T>C
XM_005251479.3:c.-115+2064T>C	XP_005251536.1:n.-115+2064T>C
XM_006716778.2:c.-5T>C	XP_006716841.1:n.-5T>C
XM_011517889.1:c.-115+2064T>C	XP_011516191.1:n.-115+2064T>C
XM_011517890.1:c.-115+2064T>C	XP_011516192.1:n.-115+2064T>C
XM_011517891.1:c.-115+2064T>C	XP_011516193.1:n.-115+2064T>C
XM_011517892.1:c.-115+2064T>C	XP_011516194.1:n.-115+2064T>C
XM_011517893.1:c.-115+2064T>C	XP_011516195.1:n.-115+2064T>C
XM_011517894.1:c.-115+2064T>C	XP_011516196.1:n.-115+2064T>C
XM_024447556.1:c.-5T>C	XP_024303324.1:n.-5T>C
XM_024447557.1:c.-5T>C	XP_024303325.1:n.-5T>C
XM_024447558.1:c.-115+2064T>C	XP_024303326.1:n.-115+2064T>C
NM_003995.4:c.-5T>C MANE Select	NP_003986.2:n.-5T>C
NM_001378923.1:c.-5T>C	NP_001365852.1:n.-5T>C