Canonical Allele Identifier: CA373371462

Gene: NPR2

Linked Data

• MyVariant Identifiers: chr9:g.35801078A>T (hg19) ; chr9:g.35801081A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35801081A>T , CM000671.2:g.35801081A>T	GRCh38
NC_000009.11:g.35801078A>T , CM000671.1:g.35801078A>T	GRCh37
NC_000009.10:g.35791078A>T	NCBI36
NG_009249.1:g.13673A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000448821.6:c.1363A>T	ENSP00000402902.2:p.Thr455Ser
ENST00000685871.1:c.1363A>T	ENSP00000509964.1:p.Thr455Ser
ENST00000686159.1:n.1402A>T
ENST00000686486.1:n.371A>T
ENST00000687302.1:n.1449A>T
ENST00000687357.1:c.1363A>T	ENSP00000509549.1:p.Thr455Ser
ENST00000687625.1:n.518A>T
ENST00000687787.1:c.1363A>T	ENSP00000509440.1:p.Thr455Ser
ENST00000688201.1:n.1395A>T
ENST00000688226.1:n.1295A>T
ENST00000688869.1:n.1669A>T
ENST00000689788.1:c.1157A>T	ENSP00000508973.1:n.1157A>T
ENST00000689898.1:c.1367A>T	ENSP00000509651.1:p.Asn456Ile
ENST00000690070.1:c.1363A>T	ENSP00000509654.1:p.Thr455Ser
ENST00000690267.1:c.1227A>T	ENSP00000510432.1:n.1227A>T
ENST00000690552.1:n.1224A>T
ENST00000691138.1:n.1224A>T
ENST00000691969.1:c.938A>T	ENSP00000510244.1:n.938A>T
ENST00000692232.1:n.2519A>T
ENST00000692233.1:c.1227A>T	ENSP00000509698.1:n.1227A>T
ENST00000692380.1:n.518A>T
ENST00000692447.1:n.2479A>T
ENST00000693094.1:c.1363A>T	ENSP00000510161.1:p.Thr455Ser
ENST00000342694.7:c.1363A>T MANE Select	ENSP00000341083.2:p.Thr455Ser
ENST00000342694.6:c.1363A>T	ENSP00000341083.2:p.Thr455Ser
ENST00000464810.5:n.1363A>T
NM_003995.3:c.1363A>T	NP_003986.2:p.Thr455Ser
XM_005251478.3:c.1363A>T	XP_005251535.1:p.Thr455Ser
XM_005251479.3:c.376A>T	XP_005251536.1:p.Thr126Ser
XM_006716778.2:c.1363A>T	XP_006716841.1:p.Thr455Ser
XM_011517889.1:c.376A>T	XP_011516191.1:p.Thr126Ser
XM_011517890.1:c.376A>T	XP_011516192.1:p.Thr126Ser
XM_011517891.1:c.376A>T	XP_011516193.1:p.Thr126Ser
XM_011517892.1:c.376A>T	XP_011516194.1:p.Thr126Ser
XM_011517893.1:c.376A>T	XP_011516195.1:p.Thr126Ser
XM_011517894.1:c.376A>T	XP_011516196.1:p.Thr126Ser
XM_011517895.1:c.-42A>T	XP_011516197.1:n.-42A>T
XM_024447556.1:c.1363A>T	XP_024303324.1:p.Thr455Ser
XM_024447557.1:c.1363A>T	XP_024303325.1:p.Thr455Ser
XM_024447558.1:c.376A>T	XP_024303326.1:p.Thr126Ser
XM_024447559.1:c.-42A>T	XP_024303327.1:n.-42A>T
XM_024447560.1:c.-42A>T	XP_024303328.1:n.-42A>T
XM_024447561.1:c.-42A>T	XP_024303329.1:n.-42A>T
NM_003995.4:c.1363A>T MANE Select	NP_003986.2:p.Thr455Ser
NM_001378923.1:c.1363A>T	NP_001365852.1:p.Thr455Ser