Canonical Allele Identifier: CA373378749

Gene: NPR2

Linked Data

• ClinVar Variation Id: 1459715
• ClinVar RCV Id: RCV001959140
• dbSNP Id: rs2132090998
• MyVariant Identifiers: chr9:g.35806079C>T (hg19) ; chr9:g.35806082C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35806082C>T , CM000671.2:g.35806082C>T	GRCh38
NC_000009.11:g.35806079C>T , CM000671.1:g.35806079C>T	GRCh37
NC_000009.10:g.35796079C>T	NCBI36
NG_009249.1:g.18674C>T
NG_047141.1:g.11191G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421267.6:c.261C>T
ENST00000448821.6:c.2221C>T	ENSP00000402902.2:p.Arg741Ter
ENST00000685871.1:c.2149C>T	ENSP00000509964.1:p.Arg717Ter
ENST00000686159.1:n.2260C>T
ENST00000686486.1:n.1391C>T
ENST00000687302.1:n.2335C>T
ENST00000687357.1:c.2074C>T	ENSP00000509549.1:p.Arg692Ter
ENST00000687625.1:n.1376C>T
ENST00000687787.1:c.2380C>T	ENSP00000509440.1:p.Arg794Ter
ENST00000688201.1:n.2178C>T
ENST00000688226.1:n.2153C>T
ENST00000688869.1:n.2527C>T
ENST00000689788.1:c.2015C>T	ENSP00000508973.1:n.2015C>T
ENST00000689898.1:c.2078C>T	ENSP00000509651.1:n.2078C>T
ENST00000690070.1:c.2305C>T	ENSP00000509654.1:p.Arg769Ter
ENST00000690267.1:c.2010C>T	ENSP00000510432.1:n.2010C>T
ENST00000690552.1:n.2082C>T
ENST00000691138.1:n.2010C>T
ENST00000691969.1:c.1721C>T	ENSP00000510244.1:n.1721C>T
ENST00000692232.1:n.3536C>T
ENST00000692233.1:c.2085C>T	ENSP00000509698.1:n.2085C>T
ENST00000692380.1:n.1376C>T
ENST00000692447.1:n.3337C>T
ENST00000693094.1:c.2221C>T	ENSP00000510161.1:p.Arg741Ter
ENST00000342694.7:c.2221C>T MANE Select	ENSP00000341083.2:p.Arg741Ter
ENST00000342694.6:c.2221C>T	ENSP00000341083.2:p.Arg741Ter
ENST00000421267.5:c.261C>T
ENST00000464810.5:n.2221C>T
NM_003995.3:c.2221C>T	NP_003986.2:p.Arg741Ter
XM_005251478.3:c.2230C>T	XP_005251535.1:p.Arg744Ter
XM_005251479.3:c.1243C>T	XP_005251536.1:p.Arg415Ter
XM_006716778.2:c.2158C>T	XP_006716841.1:p.Arg720Ter
XM_011517889.1:c.1243C>T	XP_011516191.1:p.Arg415Ter
XM_011517890.1:c.1243C>T	XP_011516192.1:p.Arg415Ter
XM_011517891.1:c.1243C>T	XP_011516193.1:p.Arg415Ter
XM_011517892.1:c.1243C>T	XP_011516194.1:p.Arg415Ter
XM_011517893.1:c.1243C>T	XP_011516195.1:p.Arg415Ter
XM_011517894.1:c.1243C>T	XP_011516196.1:p.Arg415Ter
XM_011517895.1:c.826C>T	XP_011516197.1:p.Arg276Ter
XM_024447556.1:c.2389C>T	XP_024303324.1:p.Arg797Ter
XM_024447557.1:c.2380C>T	XP_024303325.1:p.Arg794Ter
XM_024447558.1:c.1402C>T	XP_024303326.1:p.Arg468Ter
XM_024447559.1:c.985C>T	XP_024303327.1:p.Arg329Ter
XM_024447560.1:c.976C>T	XP_024303328.1:p.Arg326Ter
XM_024447561.1:c.817C>T	XP_024303329.1:p.Arg273Ter
NM_003995.4:c.2221C>T MANE Select	NP_003986.2:p.Arg741Ter
NM_001378923.1:c.2230C>T	NP_001365852.1:p.Arg744Ter