Canonical Allele Identifier: CA373378816

Gene: NPR2

Linked Data

• MyVariant Identifiers: chr9:g.35806102C>G (hg19) ; chr9:g.35806105C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35806105C>G , CM000671.2:g.35806105C>G	GRCh38
NC_000009.11:g.35806102C>G , CM000671.1:g.35806102C>G	GRCh37
NC_000009.10:g.35796102C>G	NCBI36
NG_009249.1:g.18697C>G
NG_047141.1:g.11168G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421267.6:c.284C>G
ENST00000448821.6:c.2244C>G	ENSP00000402902.2:p.Phe748Leu
ENST00000685871.1:c.2172C>G	ENSP00000509964.1:p.Phe724Leu
ENST00000686159.1:n.2283C>G
ENST00000686486.1:n.1414C>G
ENST00000687302.1:n.2358C>G
ENST00000687357.1:c.2097C>G	ENSP00000509549.1:p.Phe699Leu
ENST00000687625.1:n.1399C>G
ENST00000687787.1:c.2403C>G	ENSP00000509440.1:p.Phe801Leu
ENST00000688201.1:n.2201C>G
ENST00000688226.1:n.2176C>G
ENST00000688869.1:n.2550C>G
ENST00000689788.1:c.2038C>G	ENSP00000508973.1:n.2038C>G
ENST00000689898.1:c.2101C>G	ENSP00000509651.1:n.2101C>G
ENST00000690070.1:c.2328C>G	ENSP00000509654.1:p.Phe776Leu
ENST00000690267.1:c.2033C>G	ENSP00000510432.1:n.2033C>G
ENST00000690552.1:n.2105C>G
ENST00000691138.1:n.2033C>G
ENST00000691969.1:c.1744C>G	ENSP00000510244.1:n.1744C>G
ENST00000692232.1:n.3559C>G
ENST00000692233.1:c.2108C>G	ENSP00000509698.1:n.2108C>G
ENST00000692380.1:n.1399C>G
ENST00000692447.1:n.3360C>G
ENST00000693094.1:c.2244C>G	ENSP00000510161.1:p.Phe748Leu
ENST00000342694.7:c.2244C>G MANE Select	ENSP00000341083.2:p.Phe748Leu
ENST00000342694.6:c.2244C>G	ENSP00000341083.2:p.Phe748Leu
ENST00000421267.5:c.284C>G
ENST00000447210.5:c.21C>G	ENSP00000393029.1:p.Phe7Leu
ENST00000464810.5:n.2244C>G
NM_003995.3:c.2244C>G	NP_003986.2:p.Phe748Leu
XM_005251478.3:c.2253C>G	XP_005251535.1:p.Phe751Leu
XM_005251479.3:c.1266C>G	XP_005251536.1:p.Phe422Leu
XM_006716778.2:c.2181C>G	XP_006716841.1:p.Phe727Leu
XM_011517889.1:c.1266C>G	XP_011516191.1:p.Phe422Leu
XM_011517890.1:c.1266C>G	XP_011516192.1:p.Phe422Leu
XM_011517891.1:c.1266C>G	XP_011516193.1:p.Phe422Leu
XM_011517892.1:c.1266C>G	XP_011516194.1:p.Phe422Leu
XM_011517893.1:c.1266C>G	XP_011516195.1:p.Phe422Leu
XM_011517894.1:c.1266C>G	XP_011516196.1:p.Phe422Leu
XM_011517895.1:c.849C>G	XP_011516197.1:p.Phe283Leu
XM_024447556.1:c.2412C>G	XP_024303324.1:p.Phe804Leu
XM_024447557.1:c.2403C>G	XP_024303325.1:p.Phe801Leu
XM_024447558.1:c.1425C>G	XP_024303326.1:p.Phe475Leu
XM_024447559.1:c.1008C>G	XP_024303327.1:p.Phe336Leu
XM_024447560.1:c.999C>G	XP_024303328.1:p.Phe333Leu
XM_024447561.1:c.840C>G	XP_024303329.1:p.Phe280Leu
NM_003995.4:c.2244C>G MANE Select	NP_003986.2:p.Phe748Leu
NM_001378923.1:c.2253C>G	NP_001365852.1:p.Phe751Leu