Canonical Allele Identifier: CA373378736

Gene: NPR2

Linked Data

• MyVariant Identifiers: chr9:g.35806073A>T (hg19) ; chr9:g.35806076A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35806076A>T , CM000671.2:g.35806076A>T	GRCh38
NC_000009.11:g.35806073A>T , CM000671.1:g.35806073A>T	GRCh37
NC_000009.10:g.35796073A>T	NCBI36
NG_009249.1:g.18668A>T
NG_047141.1:g.11197T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421267.6:c.255A>T
ENST00000448821.6:c.2215A>T	ENSP00000402902.2:p.Lys739Ter
ENST00000685871.1:c.2143A>T	ENSP00000509964.1:p.Lys715Ter
ENST00000686159.1:n.2254A>T
ENST00000686486.1:n.1385A>T
ENST00000687302.1:n.2329A>T
ENST00000687357.1:c.2068A>T	ENSP00000509549.1:p.Lys690Ter
ENST00000687625.1:n.1370A>T
ENST00000687787.1:c.2374A>T	ENSP00000509440.1:p.Lys792Ter
ENST00000688201.1:n.2172A>T
ENST00000688226.1:n.2147A>T
ENST00000688869.1:n.2521A>T
ENST00000689788.1:c.2009A>T	ENSP00000508973.1:n.2009A>T
ENST00000689898.1:c.2072A>T	ENSP00000509651.1:n.2072A>T
ENST00000690070.1:c.2299A>T	ENSP00000509654.1:p.Lys767Ter
ENST00000690267.1:c.2004A>T	ENSP00000510432.1:n.2004A>T
ENST00000690552.1:n.2076A>T
ENST00000691138.1:n.2004A>T
ENST00000691969.1:c.1715A>T	ENSP00000510244.1:n.1715A>T
ENST00000692232.1:n.3530A>T
ENST00000692233.1:c.2079A>T	ENSP00000509698.1:n.2079A>T
ENST00000692380.1:n.1370A>T
ENST00000692447.1:n.3331A>T
ENST00000693094.1:c.2215A>T	ENSP00000510161.1:p.Lys739Ter
ENST00000342694.7:c.2215A>T MANE Select	ENSP00000341083.2:p.Lys739Ter
ENST00000342694.6:c.2215A>T	ENSP00000341083.2:p.Lys739Ter
ENST00000421267.5:c.255A>T
ENST00000464810.5:n.2215A>T
NM_003995.3:c.2215A>T	NP_003986.2:p.Lys739Ter
XM_005251478.3:c.2224A>T	XP_005251535.1:p.Lys742Ter
XM_005251479.3:c.1237A>T	XP_005251536.1:p.Lys413Ter
XM_006716778.2:c.2152A>T	XP_006716841.1:p.Lys718Ter
XM_011517889.1:c.1237A>T	XP_011516191.1:p.Lys413Ter
XM_011517890.1:c.1237A>T	XP_011516192.1:p.Lys413Ter
XM_011517891.1:c.1237A>T	XP_011516193.1:p.Lys413Ter
XM_011517892.1:c.1237A>T	XP_011516194.1:p.Lys413Ter
XM_011517893.1:c.1237A>T	XP_011516195.1:p.Lys413Ter
XM_011517894.1:c.1237A>T	XP_011516196.1:p.Lys413Ter
XM_011517895.1:c.820A>T	XP_011516197.1:p.Lys274Ter
XM_024447556.1:c.2383A>T	XP_024303324.1:p.Lys795Ter
XM_024447557.1:c.2374A>T	XP_024303325.1:p.Lys792Ter
XM_024447558.1:c.1396A>T	XP_024303326.1:p.Lys466Ter
XM_024447559.1:c.979A>T	XP_024303327.1:p.Lys327Ter
XM_024447560.1:c.970A>T	XP_024303328.1:p.Lys324Ter
XM_024447561.1:c.811A>T	XP_024303329.1:p.Lys271Ter
NM_003995.4:c.2215A>T MANE Select	NP_003986.2:p.Lys739Ter
NM_001378923.1:c.2224A>T	NP_001365852.1:p.Lys742Ter