Canonical Allele Identifier: CA373379467

Gene: NPR2

Linked Data

• gnomAD v4: 9-35806231-C-A
• MyVariant Identifiers: chr9:g.35806228C>A (hg19) ; chr9:g.35806231C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35806231C>A , CM000671.2:g.35806231C>A	GRCh38
NC_000009.11:g.35806228C>A , CM000671.1:g.35806228C>A	GRCh37
NC_000009.10:g.35796228C>A	NCBI36
NG_009249.1:g.18823C>A
NG_047141.1:g.11042G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421267.6:c.410C>A
ENST00000448821.6:c.2370C>A	ENSP00000402902.2:p.Asn790Lys
ENST00000685871.1:c.2298C>A	ENSP00000509964.1:p.Asn766Lys
ENST00000686159.1:n.2409C>A
ENST00000686486.1:n.1540C>A
ENST00000687302.1:n.2484C>A
ENST00000687357.1:c.2223C>A	ENSP00000509549.1:p.Asn741Lys
ENST00000687625.1:n.1525C>A
ENST00000687787.1:c.2529C>A	ENSP00000509440.1:p.Asn843Lys
ENST00000688201.1:n.2327C>A
ENST00000688226.1:n.2302C>A
ENST00000688869.1:n.2676C>A
ENST00000689788.1:c.2164C>A	ENSP00000508973.1:n.2164C>A
ENST00000689898.1:c.2227C>A	ENSP00000509651.1:n.2227C>A
ENST00000690070.1:c.2454C>A	ENSP00000509654.1:p.Asn818Lys
ENST00000690267.1:c.2159C>A	ENSP00000510432.1:n.2159C>A
ENST00000690552.1:n.2231C>A
ENST00000691138.1:n.2159C>A
ENST00000691969.1:c.1870C>A	ENSP00000510244.1:n.1870C>A
ENST00000692232.1:n.3685C>A
ENST00000692233.1:c.2234C>A	ENSP00000509698.1:n.2234C>A
ENST00000692380.1:n.1525C>A
ENST00000692447.1:n.3486C>A
ENST00000693094.1:c.2370C>A	ENSP00000510161.1:p.Asn790Lys
ENST00000342694.7:c.2370C>A MANE Select	ENSP00000341083.2:p.Asn790Lys
ENST00000342694.6:c.2370C>A	ENSP00000341083.2:p.Asn790Lys
ENST00000421267.5:c.410C>A
ENST00000447210.5:c.147C>A	ENSP00000393029.1:p.Asn49Lys
ENST00000464810.5:n.2370C>A
NM_003995.3:c.2370C>A	NP_003986.2:p.Asn790Lys
XM_005251478.3:c.2379C>A	XP_005251535.1:p.Asn793Lys
XM_005251479.3:c.1392C>A	XP_005251536.1:p.Asn464Lys
XM_006716778.2:c.2307C>A	XP_006716841.1:p.Asn769Lys
XM_011517889.1:c.1392C>A	XP_011516191.1:p.Asn464Lys
XM_011517890.1:c.1392C>A	XP_011516192.1:p.Asn464Lys
XM_011517891.1:c.1392C>A	XP_011516193.1:p.Asn464Lys
XM_011517892.1:c.1392C>A	XP_011516194.1:p.Asn464Lys
XM_011517893.1:c.1392C>A	XP_011516195.1:p.Asn464Lys
XM_011517894.1:c.1392C>A	XP_011516196.1:p.Asn464Lys
XM_011517895.1:c.975C>A	XP_011516197.1:p.Asn325Lys
XM_024447556.1:c.2538C>A	XP_024303324.1:p.Asn846Lys
XM_024447557.1:c.2529C>A	XP_024303325.1:p.Asn843Lys
XM_024447558.1:c.1551C>A	XP_024303326.1:p.Asn517Lys
XM_024447559.1:c.1134C>A	XP_024303327.1:p.Asn378Lys
XM_024447560.1:c.1125C>A	XP_024303328.1:p.Asn375Lys
XM_024447561.1:c.966C>A	XP_024303329.1:p.Asn322Lys
NM_003995.4:c.2370C>A MANE Select	NP_003986.2:p.Asn790Lys
NM_001378923.1:c.2379C>A	NP_001365852.1:p.Asn793Lys