Canonical Allele Identifier: CA464459306

Gene: NPR2

Linked Data

• MyVariant Identifiers: chr9:g.35800729T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35800732T>G , CM000671.2:g.35800732T>G	GRCh38
NC_000009.11:g.35800729T>G , CM000671.1:g.35800729T>G	GRCh37
NC_000009.10:g.35790729T>G	NCBI36
NG_009249.1:g.13324T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000448821.6:c.1242T>G	ENSP00000402902.2:p.Ala414=
ENST00000685871.1:c.1242T>G	ENSP00000509964.1:p.Ala414=
ENST00000686159.1:n.1281T>G
ENST00000686486.1:n.250T>G
ENST00000687302.1:n.1328T>G
ENST00000687357.1:c.1242T>G	ENSP00000509549.1:p.Ala414=
ENST00000687625.1:n.397T>G
ENST00000687787.1:c.1242T>G	ENSP00000509440.1:p.Ala414=
ENST00000688201.1:n.1274T>G
ENST00000688226.1:n.1174T>G
ENST00000688869.1:n.1548T>G
ENST00000689788.1:c.1036T>G	ENSP00000508973.1:n.1036T>G
ENST00000689898.1:c.1242T>G	ENSP00000509651.1:p.Ala414=
ENST00000690070.1:c.1242T>G	ENSP00000509654.1:p.Ala414=
ENST00000690267.1:c.1106T>G	ENSP00000510432.1:n.1106T>G
ENST00000690552.1:n.1103T>G
ENST00000691138.1:n.1103T>G
ENST00000691969.1:c.817T>G	ENSP00000510244.1:n.817T>G
ENST00000692232.1:n.2398T>G
ENST00000692233.1:c.1106T>G	ENSP00000509698.1:n.1106T>G
ENST00000692380.1:n.397T>G
ENST00000692447.1:n.2354T>G
ENST00000693094.1:c.1242T>G	ENSP00000510161.1:p.Ala414=
ENST00000342694.7:c.1242T>G MANE Select	ENSP00000341083.2:p.Ala414=
ENST00000342694.6:c.1242T>G	ENSP00000341083.2:p.Ala414=
ENST00000464810.5:n.1242T>G
NM_003995.3:c.1242T>G	NP_003986.2:p.Ala414=
XM_005251478.3:c.1242T>G	XP_005251535.1:p.Ala414=
XM_005251479.3:c.255T>G	XP_005251536.1:p.Ala85=
XM_006716778.2:c.1242T>G	XP_006716841.1:p.Ala414=
XM_011517889.1:c.255T>G	XP_011516191.1:p.Ala85=
XM_011517890.1:c.255T>G	XP_011516192.1:p.Ala85=
XM_011517891.1:c.255T>G	XP_011516193.1:p.Ala85=
XM_011517892.1:c.255T>G	XP_011516194.1:p.Ala85=
XM_011517893.1:c.255T>G	XP_011516195.1:p.Ala85=
XM_011517894.1:c.255T>G	XP_011516196.1:p.Ala85=
XM_024447556.1:c.1242T>G	XP_024303324.1:p.Ala414=
XM_024447557.1:c.1242T>G	XP_024303325.1:p.Ala414=
XM_024447558.1:c.255T>G	XP_024303326.1:p.Ala85=
XM_024447560.1:c.-167T>G	XP_024303328.1:n.-167T>G
XM_024447561.1:c.-167T>G	XP_024303329.1:n.-167T>G
NM_003995.4:c.1242T>G MANE Select	NP_003986.2:p.Ala414=
NM_001378923.1:c.1242T>G	NP_001365852.1:p.Ala414=