Canonical Allele Identifier: CA373379016

Gene: NPR2

Linked Data

• MyVariant Identifiers: chr9:g.35806138G>C (hg19) ; chr9:g.35806141G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35806141G>C , CM000671.2:g.35806141G>C	GRCh38
NC_000009.11:g.35806138G>C , CM000671.1:g.35806138G>C	GRCh37
NC_000009.10:g.35796138G>C	NCBI36
NG_009249.1:g.18733G>C
NG_047141.1:g.11132C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421267.6:c.320G>C
ENST00000448821.6:c.2280G>C	ENSP00000402902.2:p.Glu760Asp
ENST00000685871.1:c.2208G>C	ENSP00000509964.1:p.Glu736Asp
ENST00000686159.1:n.2319G>C
ENST00000686486.1:n.1450G>C
ENST00000687302.1:n.2394G>C
ENST00000687357.1:c.2133G>C	ENSP00000509549.1:p.Glu711Asp
ENST00000687625.1:n.1435G>C
ENST00000687787.1:c.2439G>C	ENSP00000509440.1:p.Glu813Asp
ENST00000688201.1:n.2237G>C
ENST00000688226.1:n.2212G>C
ENST00000688869.1:n.2586G>C
ENST00000689788.1:c.2074G>C	ENSP00000508973.1:n.2074G>C
ENST00000689898.1:c.2137G>C	ENSP00000509651.1:n.2137G>C
ENST00000690070.1:c.2364G>C	ENSP00000509654.1:p.Glu788Asp
ENST00000690267.1:c.2069G>C	ENSP00000510432.1:n.2069G>C
ENST00000690552.1:n.2141G>C
ENST00000691138.1:n.2069G>C
ENST00000691969.1:c.1780G>C	ENSP00000510244.1:n.1780G>C
ENST00000692232.1:n.3595G>C
ENST00000692233.1:c.2144G>C	ENSP00000509698.1:n.2144G>C
ENST00000692380.1:n.1435G>C
ENST00000692447.1:n.3396G>C
ENST00000693094.1:c.2280G>C	ENSP00000510161.1:p.Glu760Asp
ENST00000342694.7:c.2280G>C MANE Select	ENSP00000341083.2:p.Glu760Asp
ENST00000342694.6:c.2280G>C	ENSP00000341083.2:p.Glu760Asp
ENST00000421267.5:c.320G>C
ENST00000447210.5:c.57G>C	ENSP00000393029.1:p.Glu19Asp
ENST00000464810.5:n.2280G>C
NM_003995.3:c.2280G>C	NP_003986.2:p.Glu760Asp
XM_005251478.3:c.2289G>C	XP_005251535.1:p.Glu763Asp
XM_005251479.3:c.1302G>C	XP_005251536.1:p.Glu434Asp
XM_006716778.2:c.2217G>C	XP_006716841.1:p.Glu739Asp
XM_011517889.1:c.1302G>C	XP_011516191.1:p.Glu434Asp
XM_011517890.1:c.1302G>C	XP_011516192.1:p.Glu434Asp
XM_011517891.1:c.1302G>C	XP_011516193.1:p.Glu434Asp
XM_011517892.1:c.1302G>C	XP_011516194.1:p.Glu434Asp
XM_011517893.1:c.1302G>C	XP_011516195.1:p.Glu434Asp
XM_011517894.1:c.1302G>C	XP_011516196.1:p.Glu434Asp
XM_011517895.1:c.885G>C	XP_011516197.1:p.Glu295Asp
XM_024447556.1:c.2448G>C	XP_024303324.1:p.Glu816Asp
XM_024447557.1:c.2439G>C	XP_024303325.1:p.Glu813Asp
XM_024447558.1:c.1461G>C	XP_024303326.1:p.Glu487Asp
XM_024447559.1:c.1044G>C	XP_024303327.1:p.Glu348Asp
XM_024447560.1:c.1035G>C	XP_024303328.1:p.Glu345Asp
XM_024447561.1:c.876G>C	XP_024303329.1:p.Glu292Asp
NM_003995.4:c.2280G>C MANE Select	NP_003986.2:p.Glu760Asp
NM_001378923.1:c.2289G>C	NP_001365852.1:p.Glu763Asp