Canonical Allele Identifier: CA373370921

Gene: NPR2

Linked Data

• gnomAD v4: 9-35800720-C-G
• MyVariant Identifiers: chr9:g.35800717C>G (hg19) ; chr9:g.35800720C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35800720C>G , CM000671.2:g.35800720C>G	GRCh38
NC_000009.11:g.35800717C>G , CM000671.1:g.35800717C>G	GRCh37
NC_000009.10:g.35790717C>G	NCBI36
NG_009249.1:g.13312C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000448821.6:c.1230C>G	ENSP00000402902.2:p.His410Gln
ENST00000685871.1:c.1230C>G	ENSP00000509964.1:p.His410Gln
ENST00000686159.1:n.1269C>G
ENST00000686486.1:n.238C>G
ENST00000687302.1:n.1316C>G
ENST00000687357.1:c.1230C>G	ENSP00000509549.1:p.His410Gln
ENST00000687625.1:n.385C>G
ENST00000687787.1:c.1230C>G	ENSP00000509440.1:p.His410Gln
ENST00000688201.1:n.1262C>G
ENST00000688226.1:n.1162C>G
ENST00000688869.1:n.1536C>G
ENST00000689788.1:c.1024C>G	ENSP00000508973.1:n.1024C>G
ENST00000689898.1:c.1230C>G	ENSP00000509651.1:p.His410Gln
ENST00000690070.1:c.1230C>G	ENSP00000509654.1:p.His410Gln
ENST00000690267.1:c.1094C>G	ENSP00000510432.1:n.1094C>G
ENST00000690552.1:n.1091C>G
ENST00000691138.1:n.1091C>G
ENST00000691969.1:c.805C>G	ENSP00000510244.1:n.805C>G
ENST00000692232.1:n.2386C>G
ENST00000692233.1:c.1094C>G	ENSP00000509698.1:n.1094C>G
ENST00000692380.1:n.385C>G
ENST00000692447.1:n.2342C>G
ENST00000693094.1:c.1230C>G	ENSP00000510161.1:p.His410Gln
ENST00000342694.7:c.1230C>G MANE Select	ENSP00000341083.2:p.His410Gln
ENST00000342694.6:c.1230C>G	ENSP00000341083.2:p.His410Gln
ENST00000464810.5:n.1230C>G
NM_003995.3:c.1230C>G	NP_003986.2:p.His410Gln
XM_005251478.3:c.1230C>G	XP_005251535.1:p.His410Gln
XM_005251479.3:c.243C>G	XP_005251536.1:p.His81Gln
XM_006716778.2:c.1230C>G	XP_006716841.1:p.His410Gln
XM_011517889.1:c.243C>G	XP_011516191.1:p.His81Gln
XM_011517890.1:c.243C>G	XP_011516192.1:p.His81Gln
XM_011517891.1:c.243C>G	XP_011516193.1:p.His81Gln
XM_011517892.1:c.243C>G	XP_011516194.1:p.His81Gln
XM_011517893.1:c.243C>G	XP_011516195.1:p.His81Gln
XM_011517894.1:c.243C>G	XP_011516196.1:p.His81Gln
XM_024447556.1:c.1230C>G	XP_024303324.1:p.His410Gln
XM_024447557.1:c.1230C>G	XP_024303325.1:p.His410Gln
XM_024447558.1:c.243C>G	XP_024303326.1:p.His81Gln
XM_024447560.1:c.-179C>G	XP_024303328.1:n.-179C>G
XM_024447561.1:c.-179C>G	XP_024303329.1:n.-179C>G
NM_003995.4:c.1230C>G MANE Select	NP_003986.2:p.His410Gln
NM_001378923.1:c.1230C>G	NP_001365852.1:p.His410Gln