Canonical Allele Identifier: CA373371089

Gene: NPR2

Linked Data

• dbSNP Id: rs1828120901
• MyVariant Identifiers: chr9:g.35800761T>C (hg19) ; chr9:g.35800764T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35800764T>C , CM000671.2:g.35800764T>C	GRCh38
NC_000009.11:g.35800761T>C , CM000671.1:g.35800761T>C	GRCh37
NC_000009.10:g.35790761T>C	NCBI36
NG_009249.1:g.13356T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000448821.6:c.1274T>C	ENSP00000402902.2:p.Ile425Thr
ENST00000685871.1:c.1274T>C	ENSP00000509964.1:p.Ile425Thr
ENST00000686159.1:n.1313T>C
ENST00000686486.1:n.282T>C
ENST00000687302.1:n.1360T>C
ENST00000687357.1:c.1274T>C	ENSP00000509549.1:p.Ile425Thr
ENST00000687625.1:n.429T>C
ENST00000687787.1:c.1274T>C	ENSP00000509440.1:p.Ile425Thr
ENST00000688201.1:n.1306T>C
ENST00000688226.1:n.1206T>C
ENST00000688869.1:n.1580T>C
ENST00000689788.1:c.1068T>C	ENSP00000508973.1:n.1068T>C
ENST00000689898.1:c.1274T>C	ENSP00000509651.1:p.Ile425Thr
ENST00000690070.1:c.1274T>C	ENSP00000509654.1:p.Ile425Thr
ENST00000690267.1:c.1138T>C	ENSP00000510432.1:n.1138T>C
ENST00000690552.1:n.1135T>C
ENST00000691138.1:n.1135T>C
ENST00000691969.1:c.849T>C	ENSP00000510244.1:n.849T>C
ENST00000692232.1:n.2430T>C
ENST00000692233.1:c.1138T>C	ENSP00000509698.1:n.1138T>C
ENST00000692380.1:n.429T>C
ENST00000692447.1:n.2386T>C
ENST00000693094.1:c.1274T>C	ENSP00000510161.1:p.Ile425Thr
ENST00000342694.7:c.1274T>C MANE Select	ENSP00000341083.2:p.Ile425Thr
ENST00000342694.6:c.1274T>C	ENSP00000341083.2:p.Ile425Thr
ENST00000464810.5:n.1274T>C
NM_003995.3:c.1274T>C	NP_003986.2:p.Ile425Thr
XM_005251478.3:c.1274T>C	XP_005251535.1:p.Ile425Thr
XM_005251479.3:c.287T>C	XP_005251536.1:p.Ile96Thr
XM_006716778.2:c.1274T>C	XP_006716841.1:p.Ile425Thr
XM_011517889.1:c.287T>C	XP_011516191.1:p.Ile96Thr
XM_011517890.1:c.287T>C	XP_011516192.1:p.Ile96Thr
XM_011517891.1:c.287T>C	XP_011516193.1:p.Ile96Thr
XM_011517892.1:c.287T>C	XP_011516194.1:p.Ile96Thr
XM_011517893.1:c.287T>C	XP_011516195.1:p.Ile96Thr
XM_011517894.1:c.287T>C	XP_011516196.1:p.Ile96Thr
XM_011517895.1:c.-135T>C	XP_011516197.1:n.-135T>C
XM_024447556.1:c.1274T>C	XP_024303324.1:p.Ile425Thr
XM_024447557.1:c.1274T>C	XP_024303325.1:p.Ile425Thr
XM_024447558.1:c.287T>C	XP_024303326.1:p.Ile96Thr
XM_024447559.1:c.-135T>C	XP_024303327.1:n.-135T>C
XM_024447560.1:c.-135T>C	XP_024303328.1:n.-135T>C
XM_024447561.1:c.-135T>C	XP_024303329.1:n.-135T>C
NM_003995.4:c.1274T>C MANE Select	NP_003986.2:p.Ile425Thr
NM_001378923.1:c.1274T>C	NP_001365852.1:p.Ile425Thr