Canonical Allele Identifier: CA373379149

Gene: NPR2

Linked Data

• MyVariant Identifiers: chr9:g.35806162T>A (hg19) ; chr9:g.35806165T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35806165T>A , CM000671.2:g.35806165T>A	GRCh38
NC_000009.11:g.35806162T>A , CM000671.1:g.35806162T>A	GRCh37
NC_000009.10:g.35796162T>A	NCBI36
NG_009249.1:g.18757T>A
NG_047141.1:g.11108A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421267.6:c.344T>A
ENST00000448821.6:c.2304T>A	ENSP00000402902.2:p.Cys768Ter
ENST00000685871.1:c.2232T>A	ENSP00000509964.1:p.Cys744Ter
ENST00000686159.1:n.2343T>A
ENST00000686486.1:n.1474T>A
ENST00000687302.1:n.2418T>A
ENST00000687357.1:c.2157T>A	ENSP00000509549.1:p.Cys719Ter
ENST00000687625.1:n.1459T>A
ENST00000687787.1:c.2463T>A	ENSP00000509440.1:p.Cys821Ter
ENST00000688201.1:n.2261T>A
ENST00000688226.1:n.2236T>A
ENST00000688869.1:n.2610T>A
ENST00000689788.1:c.2098T>A	ENSP00000508973.1:n.2098T>A
ENST00000689898.1:c.2161T>A	ENSP00000509651.1:n.2161T>A
ENST00000690070.1:c.2388T>A	ENSP00000509654.1:p.Cys796Ter
ENST00000690267.1:c.2093T>A	ENSP00000510432.1:n.2093T>A
ENST00000690552.1:n.2165T>A
ENST00000691138.1:n.2093T>A
ENST00000691969.1:c.1804T>A	ENSP00000510244.1:n.1804T>A
ENST00000692232.1:n.3619T>A
ENST00000692233.1:c.2168T>A	ENSP00000509698.1:n.2168T>A
ENST00000692380.1:n.1459T>A
ENST00000692447.1:n.3420T>A
ENST00000693094.1:c.2304T>A	ENSP00000510161.1:p.Cys768Ter
ENST00000342694.7:c.2304T>A MANE Select	ENSP00000341083.2:p.Cys768Ter
ENST00000342694.6:c.2304T>A	ENSP00000341083.2:p.Cys768Ter
ENST00000421267.5:c.344T>A
ENST00000447210.5:c.81T>A	ENSP00000393029.1:p.Cys27Ter
ENST00000464810.5:n.2304T>A
NM_003995.3:c.2304T>A	NP_003986.2:p.Cys768Ter
XM_005251478.3:c.2313T>A	XP_005251535.1:p.Cys771Ter
XM_005251479.3:c.1326T>A	XP_005251536.1:p.Cys442Ter
XM_006716778.2:c.2241T>A	XP_006716841.1:p.Cys747Ter
XM_011517889.1:c.1326T>A	XP_011516191.1:p.Cys442Ter
XM_011517890.1:c.1326T>A	XP_011516192.1:p.Cys442Ter
XM_011517891.1:c.1326T>A	XP_011516193.1:p.Cys442Ter
XM_011517892.1:c.1326T>A	XP_011516194.1:p.Cys442Ter
XM_011517893.1:c.1326T>A	XP_011516195.1:p.Cys442Ter
XM_011517894.1:c.1326T>A	XP_011516196.1:p.Cys442Ter
XM_011517895.1:c.909T>A	XP_011516197.1:p.Cys303Ter
XM_024447556.1:c.2472T>A	XP_024303324.1:p.Cys824Ter
XM_024447557.1:c.2463T>A	XP_024303325.1:p.Cys821Ter
XM_024447558.1:c.1485T>A	XP_024303326.1:p.Cys495Ter
XM_024447559.1:c.1068T>A	XP_024303327.1:p.Cys356Ter
XM_024447560.1:c.1059T>A	XP_024303328.1:p.Cys353Ter
XM_024447561.1:c.900T>A	XP_024303329.1:p.Cys300Ter
NM_003995.4:c.2304T>A MANE Select	NP_003986.2:p.Cys768Ter
NM_001378923.1:c.2313T>A	NP_001365852.1:p.Cys771Ter