Canonical Allele Identifier: CA464465028

Gene: NPR2

Linked Data

• MyVariant Identifiers: chr9:g.35806210C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35806213C>G , CM000671.2:g.35806213C>G	GRCh38
NC_000009.11:g.35806210C>G , CM000671.1:g.35806210C>G	GRCh37
NC_000009.10:g.35796210C>G	NCBI36
NG_009249.1:g.18805C>G
NG_047141.1:g.11060G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421267.6:c.392C>G
ENST00000448821.6:c.2352C>G	ENSP00000402902.2:p.Gly784=
ENST00000685871.1:c.2280C>G	ENSP00000509964.1:p.Gly760=
ENST00000686159.1:n.2391C>G
ENST00000686486.1:n.1522C>G
ENST00000687302.1:n.2466C>G
ENST00000687357.1:c.2205C>G	ENSP00000509549.1:p.Gly735=
ENST00000687625.1:n.1507C>G
ENST00000687787.1:c.2511C>G	ENSP00000509440.1:p.Gly837=
ENST00000688201.1:n.2309C>G
ENST00000688226.1:n.2284C>G
ENST00000688869.1:n.2658C>G
ENST00000689788.1:c.2146C>G	ENSP00000508973.1:n.2146C>G
ENST00000689898.1:c.2209C>G	ENSP00000509651.1:n.2209C>G
ENST00000690070.1:c.2436C>G	ENSP00000509654.1:p.Gly812=
ENST00000690267.1:c.2141C>G	ENSP00000510432.1:n.2141C>G
ENST00000690552.1:n.2213C>G
ENST00000691138.1:n.2141C>G
ENST00000691969.1:c.1852C>G	ENSP00000510244.1:n.1852C>G
ENST00000692232.1:n.3667C>G
ENST00000692233.1:c.2216C>G	ENSP00000509698.1:n.2216C>G
ENST00000692380.1:n.1507C>G
ENST00000692447.1:n.3468C>G
ENST00000693094.1:c.2352C>G	ENSP00000510161.1:p.Gly784=
ENST00000342694.7:c.2352C>G MANE Select	ENSP00000341083.2:p.Gly784=
ENST00000342694.6:c.2352C>G	ENSP00000341083.2:p.Gly784=
ENST00000421267.5:c.392C>G
ENST00000447210.5:c.129C>G	ENSP00000393029.1:p.Gly43=
ENST00000464810.5:n.2352C>G
NM_003995.3:c.2352C>G	NP_003986.2:p.Gly784=
XM_005251478.3:c.2361C>G	XP_005251535.1:p.Gly787=
XM_005251479.3:c.1374C>G	XP_005251536.1:p.Gly458=
XM_006716778.2:c.2289C>G	XP_006716841.1:p.Gly763=
XM_011517889.1:c.1374C>G	XP_011516191.1:p.Gly458=
XM_011517890.1:c.1374C>G	XP_011516192.1:p.Gly458=
XM_011517891.1:c.1374C>G	XP_011516193.1:p.Gly458=
XM_011517892.1:c.1374C>G	XP_011516194.1:p.Gly458=
XM_011517893.1:c.1374C>G	XP_011516195.1:p.Gly458=
XM_011517894.1:c.1374C>G	XP_011516196.1:p.Gly458=
XM_011517895.1:c.957C>G	XP_011516197.1:p.Gly319=
XM_024447556.1:c.2520C>G	XP_024303324.1:p.Gly840=
XM_024447557.1:c.2511C>G	XP_024303325.1:p.Gly837=
XM_024447558.1:c.1533C>G	XP_024303326.1:p.Gly511=
XM_024447559.1:c.1116C>G	XP_024303327.1:p.Gly372=
XM_024447560.1:c.1107C>G	XP_024303328.1:p.Gly369=
XM_024447561.1:c.948C>G	XP_024303329.1:p.Gly316=
NM_003995.4:c.2352C>G MANE Select	NP_003986.2:p.Gly784=
NM_001378923.1:c.2361C>G	NP_001365852.1:p.Gly787=