Canonical Allele Identifier: CA373379198

Gene: NPR2

Linked Data

• MyVariant Identifiers: chr9:g.35806172G>T (hg19) ; chr9:g.35806175G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35806175G>T , CM000671.2:g.35806175G>T	GRCh38
NC_000009.11:g.35806172G>T , CM000671.1:g.35806172G>T	GRCh37
NC_000009.10:g.35796172G>T	NCBI36
NG_009249.1:g.18767G>T
NG_047141.1:g.11098C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421267.6:c.354G>T
ENST00000448821.6:c.2314G>T	ENSP00000402902.2:p.Asp772Tyr
ENST00000685871.1:c.2242G>T	ENSP00000509964.1:p.Asp748Tyr
ENST00000686159.1:n.2353G>T
ENST00000686486.1:n.1484G>T
ENST00000687302.1:n.2428G>T
ENST00000687357.1:c.2167G>T	ENSP00000509549.1:p.Asp723Tyr
ENST00000687625.1:n.1469G>T
ENST00000687787.1:c.2473G>T	ENSP00000509440.1:p.Asp825Tyr
ENST00000688201.1:n.2271G>T
ENST00000688226.1:n.2246G>T
ENST00000688869.1:n.2620G>T
ENST00000689788.1:c.2108G>T	ENSP00000508973.1:n.2108G>T
ENST00000689898.1:c.2171G>T	ENSP00000509651.1:n.2171G>T
ENST00000690070.1:c.2398G>T	ENSP00000509654.1:p.Asp800Tyr
ENST00000690267.1:c.2103G>T	ENSP00000510432.1:n.2103G>T
ENST00000690552.1:n.2175G>T
ENST00000691138.1:n.2103G>T
ENST00000691969.1:c.1814G>T	ENSP00000510244.1:n.1814G>T
ENST00000692232.1:n.3629G>T
ENST00000692233.1:c.2178G>T	ENSP00000509698.1:n.2178G>T
ENST00000692380.1:n.1469G>T
ENST00000692447.1:n.3430G>T
ENST00000693094.1:c.2314G>T	ENSP00000510161.1:p.Asp772Tyr
ENST00000342694.7:c.2314G>T MANE Select	ENSP00000341083.2:p.Asp772Tyr
ENST00000342694.6:c.2314G>T	ENSP00000341083.2:p.Asp772Tyr
ENST00000421267.5:c.354G>T
ENST00000447210.5:c.91G>T	ENSP00000393029.1:p.Asp31Tyr
ENST00000464810.5:n.2314G>T
NM_003995.3:c.2314G>T	NP_003986.2:p.Asp772Tyr
XM_005251478.3:c.2323G>T	XP_005251535.1:p.Asp775Tyr
XM_005251479.3:c.1336G>T	XP_005251536.1:p.Asp446Tyr
XM_006716778.2:c.2251G>T	XP_006716841.1:p.Asp751Tyr
XM_011517889.1:c.1336G>T	XP_011516191.1:p.Asp446Tyr
XM_011517890.1:c.1336G>T	XP_011516192.1:p.Asp446Tyr
XM_011517891.1:c.1336G>T	XP_011516193.1:p.Asp446Tyr
XM_011517892.1:c.1336G>T	XP_011516194.1:p.Asp446Tyr
XM_011517893.1:c.1336G>T	XP_011516195.1:p.Asp446Tyr
XM_011517894.1:c.1336G>T	XP_011516196.1:p.Asp446Tyr
XM_011517895.1:c.919G>T	XP_011516197.1:p.Asp307Tyr
XM_024447556.1:c.2482G>T	XP_024303324.1:p.Asp828Tyr
XM_024447557.1:c.2473G>T	XP_024303325.1:p.Asp825Tyr
XM_024447558.1:c.1495G>T	XP_024303326.1:p.Asp499Tyr
XM_024447559.1:c.1078G>T	XP_024303327.1:p.Asp360Tyr
XM_024447560.1:c.1069G>T	XP_024303328.1:p.Asp357Tyr
XM_024447561.1:c.910G>T	XP_024303329.1:p.Asp304Tyr
NM_003995.4:c.2314G>T MANE Select	NP_003986.2:p.Asp772Tyr
NM_001378923.1:c.2323G>T	NP_001365852.1:p.Asp775Tyr