Canonical Allele Identifier: CA464615738

Gene: NPR2

Linked Data

• MyVariant Identifiers: chr9:g.35806168T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35806171T>G , CM000671.2:g.35806171T>G	GRCh38
NC_000009.11:g.35806168T>G , CM000671.1:g.35806168T>G	GRCh37
NC_000009.10:g.35796168T>G	NCBI36
NG_009249.1:g.18763T>G
NG_047141.1:g.11102A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421267.6:c.350T>G
ENST00000448821.6:c.2310T>G	ENSP00000402902.2:p.Ala770=
ENST00000685871.1:c.2238T>G	ENSP00000509964.1:p.Ala746=
ENST00000686159.1:n.2349T>G
ENST00000686486.1:n.1480T>G
ENST00000687302.1:n.2424T>G
ENST00000687357.1:c.2163T>G	ENSP00000509549.1:p.Ala721=
ENST00000687625.1:n.1465T>G
ENST00000687787.1:c.2469T>G	ENSP00000509440.1:p.Ala823=
ENST00000688201.1:n.2267T>G
ENST00000688226.1:n.2242T>G
ENST00000688869.1:n.2616T>G
ENST00000689788.1:c.2104T>G	ENSP00000508973.1:n.2104T>G
ENST00000689898.1:c.2167T>G	ENSP00000509651.1:n.2167T>G
ENST00000690070.1:c.2394T>G	ENSP00000509654.1:p.Ala798=
ENST00000690267.1:c.2099T>G	ENSP00000510432.1:n.2099T>G
ENST00000690552.1:n.2171T>G
ENST00000691138.1:n.2099T>G
ENST00000691969.1:c.1810T>G	ENSP00000510244.1:n.1810T>G
ENST00000692232.1:n.3625T>G
ENST00000692233.1:c.2174T>G	ENSP00000509698.1:n.2174T>G
ENST00000692380.1:n.1465T>G
ENST00000692447.1:n.3426T>G
ENST00000693094.1:c.2310T>G	ENSP00000510161.1:p.Ala770=
ENST00000342694.7:c.2310T>G MANE Select	ENSP00000341083.2:p.Ala770=
ENST00000342694.6:c.2310T>G	ENSP00000341083.2:p.Ala770=
ENST00000421267.5:c.350T>G
ENST00000447210.5:c.87T>G	ENSP00000393029.1:p.Ala29=
ENST00000464810.5:n.2310T>G
NM_003995.3:c.2310T>G	NP_003986.2:p.Ala770=
XM_005251478.3:c.2319T>G	XP_005251535.1:p.Ala773=
XM_005251479.3:c.1332T>G	XP_005251536.1:p.Ala444=
XM_006716778.2:c.2247T>G	XP_006716841.1:p.Ala749=
XM_011517889.1:c.1332T>G	XP_011516191.1:p.Ala444=
XM_011517890.1:c.1332T>G	XP_011516192.1:p.Ala444=
XM_011517891.1:c.1332T>G	XP_011516193.1:p.Ala444=
XM_011517892.1:c.1332T>G	XP_011516194.1:p.Ala444=
XM_011517893.1:c.1332T>G	XP_011516195.1:p.Ala444=
XM_011517894.1:c.1332T>G	XP_011516196.1:p.Ala444=
XM_011517895.1:c.915T>G	XP_011516197.1:p.Ala305=
XM_024447556.1:c.2478T>G	XP_024303324.1:p.Ala826=
XM_024447557.1:c.2469T>G	XP_024303325.1:p.Ala823=
XM_024447558.1:c.1491T>G	XP_024303326.1:p.Ala497=
XM_024447559.1:c.1074T>G	XP_024303327.1:p.Ala358=
XM_024447560.1:c.1065T>G	XP_024303328.1:p.Ala355=
XM_024447561.1:c.906T>G	XP_024303329.1:p.Ala302=
NM_003995.4:c.2310T>G MANE Select	NP_003986.2:p.Ala770=
NM_001378923.1:c.2319T>G	NP_001365852.1:p.Ala773=