Canonical Allele Identifier: CA373378915

Gene: NPR2

Linked Data

• MyVariant Identifiers: chr9:g.35806122C>G (hg19) ; chr9:g.35806125C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35806125C>G , CM000671.2:g.35806125C>G	GRCh38
NC_000009.11:g.35806122C>G , CM000671.1:g.35806122C>G	GRCh37
NC_000009.10:g.35796122C>G	NCBI36
NG_009249.1:g.18717C>G
NG_047141.1:g.11148G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421267.6:c.304C>G
ENST00000448821.6:c.2264C>G	ENSP00000402902.2:p.Thr755Ser
ENST00000685871.1:c.2192C>G	ENSP00000509964.1:p.Thr731Ser
ENST00000686159.1:n.2303C>G
ENST00000686486.1:n.1434C>G
ENST00000687302.1:n.2378C>G
ENST00000687357.1:c.2117C>G	ENSP00000509549.1:p.Thr706Ser
ENST00000687625.1:n.1419C>G
ENST00000687787.1:c.2423C>G	ENSP00000509440.1:p.Thr808Ser
ENST00000688201.1:n.2221C>G
ENST00000688226.1:n.2196C>G
ENST00000688869.1:n.2570C>G
ENST00000689788.1:c.2058C>G	ENSP00000508973.1:n.2058C>G
ENST00000689898.1:c.2121C>G	ENSP00000509651.1:n.2121C>G
ENST00000690070.1:c.2348C>G	ENSP00000509654.1:p.Thr783Ser
ENST00000690267.1:c.2053C>G	ENSP00000510432.1:n.2053C>G
ENST00000690552.1:n.2125C>G
ENST00000691138.1:n.2053C>G
ENST00000691969.1:c.1764C>G	ENSP00000510244.1:n.1764C>G
ENST00000692232.1:n.3579C>G
ENST00000692233.1:c.2128C>G	ENSP00000509698.1:n.2128C>G
ENST00000692380.1:n.1419C>G
ENST00000692447.1:n.3380C>G
ENST00000693094.1:c.2264C>G	ENSP00000510161.1:p.Thr755Ser
ENST00000342694.7:c.2264C>G MANE Select	ENSP00000341083.2:p.Thr755Ser
ENST00000342694.6:c.2264C>G	ENSP00000341083.2:p.Thr755Ser
ENST00000421267.5:c.304C>G
ENST00000447210.5:c.41C>G	ENSP00000393029.1:p.Thr14Ser
ENST00000464810.5:n.2264C>G
NM_003995.3:c.2264C>G	NP_003986.2:p.Thr755Ser
XM_005251478.3:c.2273C>G	XP_005251535.1:p.Thr758Ser
XM_005251479.3:c.1286C>G	XP_005251536.1:p.Thr429Ser
XM_006716778.2:c.2201C>G	XP_006716841.1:p.Thr734Ser
XM_011517889.1:c.1286C>G	XP_011516191.1:p.Thr429Ser
XM_011517890.1:c.1286C>G	XP_011516192.1:p.Thr429Ser
XM_011517891.1:c.1286C>G	XP_011516193.1:p.Thr429Ser
XM_011517892.1:c.1286C>G	XP_011516194.1:p.Thr429Ser
XM_011517893.1:c.1286C>G	XP_011516195.1:p.Thr429Ser
XM_011517894.1:c.1286C>G	XP_011516196.1:p.Thr429Ser
XM_011517895.1:c.869C>G	XP_011516197.1:p.Thr290Ser
XM_024447556.1:c.2432C>G	XP_024303324.1:p.Thr811Ser
XM_024447557.1:c.2423C>G	XP_024303325.1:p.Thr808Ser
XM_024447558.1:c.1445C>G	XP_024303326.1:p.Thr482Ser
XM_024447559.1:c.1028C>G	XP_024303327.1:p.Thr343Ser
XM_024447560.1:c.1019C>G	XP_024303328.1:p.Thr340Ser
XM_024447561.1:c.860C>G	XP_024303329.1:p.Thr287Ser
NM_003995.4:c.2264C>G MANE Select	NP_003986.2:p.Thr755Ser
NM_001378923.1:c.2273C>G	NP_001365852.1:p.Thr758Ser