Canonical Allele Identifier: CA373379267

Gene: NPR2

Linked Data

• MyVariant Identifiers: chr9:g.35806187C>T (hg19) ; chr9:g.35806190C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35806190C>T , CM000671.2:g.35806190C>T	GRCh38
NC_000009.11:g.35806187C>T , CM000671.1:g.35806187C>T	GRCh37
NC_000009.10:g.35796187C>T	NCBI36
NG_009249.1:g.18782C>T
NG_047141.1:g.11083G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421267.6:c.369C>T
ENST00000448821.6:c.2329C>T	ENSP00000402902.2:p.Pro777Ser
ENST00000685871.1:c.2257C>T	ENSP00000509964.1:p.Pro753Ser
ENST00000686159.1:n.2368C>T
ENST00000686486.1:n.1499C>T
ENST00000687302.1:n.2443C>T
ENST00000687357.1:c.2182C>T	ENSP00000509549.1:p.Pro728Ser
ENST00000687625.1:n.1484C>T
ENST00000687787.1:c.2488C>T	ENSP00000509440.1:p.Pro830Ser
ENST00000688201.1:n.2286C>T
ENST00000688226.1:n.2261C>T
ENST00000688869.1:n.2635C>T
ENST00000689788.1:c.2123C>T	ENSP00000508973.1:n.2123C>T
ENST00000689898.1:c.2186C>T	ENSP00000509651.1:n.2186C>T
ENST00000690070.1:c.2413C>T	ENSP00000509654.1:p.Pro805Ser
ENST00000690267.1:c.2118C>T	ENSP00000510432.1:n.2118C>T
ENST00000690552.1:n.2190C>T
ENST00000691138.1:n.2118C>T
ENST00000691969.1:c.1829C>T	ENSP00000510244.1:n.1829C>T
ENST00000692232.1:n.3644C>T
ENST00000692233.1:c.2193C>T	ENSP00000509698.1:n.2193C>T
ENST00000692380.1:n.1484C>T
ENST00000692447.1:n.3445C>T
ENST00000693094.1:c.2329C>T	ENSP00000510161.1:p.Pro777Ser
ENST00000342694.7:c.2329C>T MANE Select	ENSP00000341083.2:p.Pro777Ser
ENST00000342694.6:c.2329C>T	ENSP00000341083.2:p.Pro777Ser
ENST00000421267.5:c.369C>T
ENST00000447210.5:c.106C>T	ENSP00000393029.1:p.Pro36Ser
ENST00000464810.5:n.2329C>T
NM_003995.3:c.2329C>T	NP_003986.2:p.Pro777Ser
XM_005251478.3:c.2338C>T	XP_005251535.1:p.Pro780Ser
XM_005251479.3:c.1351C>T	XP_005251536.1:p.Pro451Ser
XM_006716778.2:c.2266C>T	XP_006716841.1:p.Pro756Ser
XM_011517889.1:c.1351C>T	XP_011516191.1:p.Pro451Ser
XM_011517890.1:c.1351C>T	XP_011516192.1:p.Pro451Ser
XM_011517891.1:c.1351C>T	XP_011516193.1:p.Pro451Ser
XM_011517892.1:c.1351C>T	XP_011516194.1:p.Pro451Ser
XM_011517893.1:c.1351C>T	XP_011516195.1:p.Pro451Ser
XM_011517894.1:c.1351C>T	XP_011516196.1:p.Pro451Ser
XM_011517895.1:c.934C>T	XP_011516197.1:p.Pro312Ser
XM_024447556.1:c.2497C>T	XP_024303324.1:p.Pro833Ser
XM_024447557.1:c.2488C>T	XP_024303325.1:p.Pro830Ser
XM_024447558.1:c.1510C>T	XP_024303326.1:p.Pro504Ser
XM_024447559.1:c.1093C>T	XP_024303327.1:p.Pro365Ser
XM_024447560.1:c.1084C>T	XP_024303328.1:p.Pro362Ser
XM_024447561.1:c.925C>T	XP_024303329.1:p.Pro309Ser
NM_003995.4:c.2329C>T MANE Select	NP_003986.2:p.Pro777Ser
NM_001378923.1:c.2338C>T	NP_001365852.1:p.Pro780Ser