Canonical Allele Identifier: CA373379462

Gene: NPR2

Linked Data

• MyVariant Identifiers: chr9:g.35806227A>G (hg19) ; chr9:g.35806230A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35806230A>G , CM000671.2:g.35806230A>G	GRCh38
NC_000009.11:g.35806227A>G , CM000671.1:g.35806227A>G	GRCh37
NC_000009.10:g.35796227A>G	NCBI36
NG_009249.1:g.18822A>G
NG_047141.1:g.11043T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421267.6:c.409A>G
ENST00000448821.6:c.2369A>G	ENSP00000402902.2:p.Asn790Ser
ENST00000685871.1:c.2297A>G	ENSP00000509964.1:p.Asn766Ser
ENST00000686159.1:n.2408A>G
ENST00000686486.1:n.1539A>G
ENST00000687302.1:n.2483A>G
ENST00000687357.1:c.2222A>G	ENSP00000509549.1:p.Asn741Ser
ENST00000687625.1:n.1524A>G
ENST00000687787.1:c.2528A>G	ENSP00000509440.1:p.Asn843Ser
ENST00000688201.1:n.2326A>G
ENST00000688226.1:n.2301A>G
ENST00000688869.1:n.2675A>G
ENST00000689788.1:c.2163A>G	ENSP00000508973.1:n.2163A>G
ENST00000689898.1:c.2226A>G	ENSP00000509651.1:n.2226A>G
ENST00000690070.1:c.2453A>G	ENSP00000509654.1:p.Asn818Ser
ENST00000690267.1:c.2158A>G	ENSP00000510432.1:n.2158A>G
ENST00000690552.1:n.2230A>G
ENST00000691138.1:n.2158A>G
ENST00000691969.1:c.1869A>G	ENSP00000510244.1:n.1869A>G
ENST00000692232.1:n.3684A>G
ENST00000692233.1:c.2233A>G	ENSP00000509698.1:n.2233A>G
ENST00000692380.1:n.1524A>G
ENST00000692447.1:n.3485A>G
ENST00000693094.1:c.2369A>G	ENSP00000510161.1:p.Asn790Ser
ENST00000342694.7:c.2369A>G MANE Select	ENSP00000341083.2:p.Asn790Ser
ENST00000342694.6:c.2369A>G	ENSP00000341083.2:p.Asn790Ser
ENST00000421267.5:c.409A>G
ENST00000447210.5:c.146A>G	ENSP00000393029.1:p.Asn49Ser
ENST00000464810.5:n.2369A>G
NM_003995.3:c.2369A>G	NP_003986.2:p.Asn790Ser
XM_005251478.3:c.2378A>G	XP_005251535.1:p.Asn793Ser
XM_005251479.3:c.1391A>G	XP_005251536.1:p.Asn464Ser
XM_006716778.2:c.2306A>G	XP_006716841.1:p.Asn769Ser
XM_011517889.1:c.1391A>G	XP_011516191.1:p.Asn464Ser
XM_011517890.1:c.1391A>G	XP_011516192.1:p.Asn464Ser
XM_011517891.1:c.1391A>G	XP_011516193.1:p.Asn464Ser
XM_011517892.1:c.1391A>G	XP_011516194.1:p.Asn464Ser
XM_011517893.1:c.1391A>G	XP_011516195.1:p.Asn464Ser
XM_011517894.1:c.1391A>G	XP_011516196.1:p.Asn464Ser
XM_011517895.1:c.974A>G	XP_011516197.1:p.Asn325Ser
XM_024447556.1:c.2537A>G	XP_024303324.1:p.Asn846Ser
XM_024447557.1:c.2528A>G	XP_024303325.1:p.Asn843Ser
XM_024447558.1:c.1550A>G	XP_024303326.1:p.Asn517Ser
XM_024447559.1:c.1133A>G	XP_024303327.1:p.Asn378Ser
XM_024447560.1:c.1124A>G	XP_024303328.1:p.Asn375Ser
XM_024447561.1:c.965A>G	XP_024303329.1:p.Asn322Ser
NM_003995.4:c.2369A>G MANE Select	NP_003986.2:p.Asn790Ser
NM_001378923.1:c.2378A>G	NP_001365852.1:p.Asn793Ser