Canonical Allele Identifier: CA5051900

Gene: NPR2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35805887T>A , CM000671.2:g.35805887T>A	GRCh38
NC_000009.11:g.35805884T>A , CM000671.1:g.35805884T>A	GRCh37
NC_000009.10:g.35795884T>A	NCBI36
NG_009249.1:g.18479T>A
NG_047141.1:g.11386A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_003995.4:c.2105T>A MANE Select	NP_003986.2:p.Met702Lys
ENST00000342694.7:c.2105T>A MANE Select	ENSP00000341083.2:p.Met702Lys
NM_001378923.1:c.2114T>A	NP_001365852.1:p.Met705Lys
NM_003995.3:c.2105T>A	NP_003986.2:p.Met702Lys
ENST00000342694.6:c.2105T>A	ENSP00000341083.2:p.Met702Lys
ENST00000421267.5:c.145T>A
ENST00000421267.6:c.145T>A
ENST00000448821.6:c.2105T>A	ENSP00000402902.2:p.Met702Lys
ENST00000464810.5:n.2105T>A
ENST00000685871.1:c.2033T>A	ENSP00000509964.1:p.Met678Lys
ENST00000686159.1:n.2144T>A
ENST00000686486.1:n.1275T>A
ENST00000687302.1:n.2219T>A
ENST00000687357.1:c.1958T>A	ENSP00000509549.1:p.Met653Lys
ENST00000687625.1:n.1260T>A
ENST00000687787.1:c.2264T>A	ENSP00000509440.1:p.Met755Lys
ENST00000688201.1:n.2062T>A
ENST00000688226.1:n.2037T>A
ENST00000688869.1:n.2411T>A
ENST00000689788.1:c.1899T>A	ENSP00000508973.1:n.1899T>A
ENST00000689898.1:c.1962T>A	ENSP00000509651.1:n.1962T>A
ENST00000690070.1:c.2189T>A	ENSP00000509654.1:p.Met730Lys
ENST00000690267.1:c.1894T>A	ENSP00000510432.1:n.1894T>A
ENST00000690552.1:n.1966T>A
ENST00000691138.1:n.1894T>A
ENST00000691969.1:c.1605T>A	ENSP00000510244.1:n.1605T>A
ENST00000692232.1:n.3420T>A
ENST00000692233.1:c.1969T>A	ENSP00000509698.1:n.1969T>A
ENST00000692380.1:n.1260T>A
ENST00000692447.1:n.3221T>A
ENST00000693094.1:c.2105T>A	ENSP00000510161.1:p.Met702Lys
XM_005251478.3:c.2114T>A	XP_005251535.1:p.Met705Lys
XM_005251479.3:c.1127T>A	XP_005251536.1:p.Met376Lys
XM_006716778.2:c.2042T>A	XP_006716841.1:p.Met681Lys
XM_011517889.1:c.1127T>A	XP_011516191.1:p.Met376Lys
XM_011517890.1:c.1127T>A	XP_011516192.1:p.Met376Lys
XM_011517891.1:c.1127T>A	XP_011516193.1:p.Met376Lys
XM_011517892.1:c.1127T>A	XP_011516194.1:p.Met376Lys
XM_011517893.1:c.1127T>A	XP_011516195.1:p.Met376Lys
XM_011517894.1:c.1127T>A	XP_011516196.1:p.Met376Lys
XM_011517895.1:c.710T>A	XP_011516197.1:p.Met237Lys
XM_024447556.1:c.2273T>A	XP_024303324.1:p.Met758Lys
XM_024447557.1:c.2264T>A	XP_024303325.1:p.Met755Lys
XM_024447558.1:c.1286T>A	XP_024303326.1:p.Met429Lys
XM_024447559.1:c.869T>A	XP_024303327.1:p.Met290Lys
XM_024447560.1:c.860T>A	XP_024303328.1:p.Met287Lys
XM_024447561.1:c.701T>A	XP_024303329.1:p.Met234Lys