Canonical Allele Identifier: CA373379231

Gene: NPR2

Linked Data

• MyVariant Identifiers: chr9:g.35806178G>C (hg19) ; chr9:g.35806181G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35806181G>C , CM000671.2:g.35806181G>C	GRCh38
NC_000009.11:g.35806178G>C , CM000671.1:g.35806178G>C	GRCh37
NC_000009.10:g.35796178G>C	NCBI36
NG_009249.1:g.18773G>C
NG_047141.1:g.11092C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421267.6:c.360G>C
ENST00000448821.6:c.2320G>C	ENSP00000402902.2:p.Ala774Pro
ENST00000685871.1:c.2248G>C	ENSP00000509964.1:p.Ala750Pro
ENST00000686159.1:n.2359G>C
ENST00000686486.1:n.1490G>C
ENST00000687302.1:n.2434G>C
ENST00000687357.1:c.2173G>C	ENSP00000509549.1:p.Ala725Pro
ENST00000687625.1:n.1475G>C
ENST00000687787.1:c.2479G>C	ENSP00000509440.1:p.Ala827Pro
ENST00000688201.1:n.2277G>C
ENST00000688226.1:n.2252G>C
ENST00000688869.1:n.2626G>C
ENST00000689788.1:c.2114G>C	ENSP00000508973.1:n.2114G>C
ENST00000689898.1:c.2177G>C	ENSP00000509651.1:n.2177G>C
ENST00000690070.1:c.2404G>C	ENSP00000509654.1:p.Ala802Pro
ENST00000690267.1:c.2109G>C	ENSP00000510432.1:n.2109G>C
ENST00000690552.1:n.2181G>C
ENST00000691138.1:n.2109G>C
ENST00000691969.1:c.1820G>C	ENSP00000510244.1:n.1820G>C
ENST00000692232.1:n.3635G>C
ENST00000692233.1:c.2184G>C	ENSP00000509698.1:n.2184G>C
ENST00000692380.1:n.1475G>C
ENST00000692447.1:n.3436G>C
ENST00000693094.1:c.2320G>C	ENSP00000510161.1:p.Ala774Pro
ENST00000342694.7:c.2320G>C MANE Select	ENSP00000341083.2:p.Ala774Pro
ENST00000342694.6:c.2320G>C	ENSP00000341083.2:p.Ala774Pro
ENST00000421267.5:c.360G>C
ENST00000447210.5:c.97G>C	ENSP00000393029.1:p.Ala33Pro
ENST00000464810.5:n.2320G>C
NM_003995.3:c.2320G>C	NP_003986.2:p.Ala774Pro
XM_005251478.3:c.2329G>C	XP_005251535.1:p.Ala777Pro
XM_005251479.3:c.1342G>C	XP_005251536.1:p.Ala448Pro
XM_006716778.2:c.2257G>C	XP_006716841.1:p.Ala753Pro
XM_011517889.1:c.1342G>C	XP_011516191.1:p.Ala448Pro
XM_011517890.1:c.1342G>C	XP_011516192.1:p.Ala448Pro
XM_011517891.1:c.1342G>C	XP_011516193.1:p.Ala448Pro
XM_011517892.1:c.1342G>C	XP_011516194.1:p.Ala448Pro
XM_011517893.1:c.1342G>C	XP_011516195.1:p.Ala448Pro
XM_011517894.1:c.1342G>C	XP_011516196.1:p.Ala448Pro
XM_011517895.1:c.925G>C	XP_011516197.1:p.Ala309Pro
XM_024447556.1:c.2488G>C	XP_024303324.1:p.Ala830Pro
XM_024447557.1:c.2479G>C	XP_024303325.1:p.Ala827Pro
XM_024447558.1:c.1501G>C	XP_024303326.1:p.Ala501Pro
XM_024447559.1:c.1084G>C	XP_024303327.1:p.Ala362Pro
XM_024447560.1:c.1075G>C	XP_024303328.1:p.Ala359Pro
XM_024447561.1:c.916G>C	XP_024303329.1:p.Ala306Pro
NM_003995.4:c.2320G>C MANE Select	NP_003986.2:p.Ala774Pro
NM_001378923.1:c.2329G>C	NP_001365852.1:p.Ala777Pro