Canonical Allele Identifier: CA464460414

Gene: NPR2

Linked Data

• MyVariant Identifiers: chr9:g.35801146T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35801149T>C , CM000671.2:g.35801149T>C	GRCh38
NC_000009.11:g.35801146T>C , CM000671.1:g.35801146T>C	GRCh37
NC_000009.10:g.35791146T>C	NCBI36
NG_009249.1:g.13741T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000448821.6:c.1431T>C	ENSP00000402902.2:p.Ile477=
ENST00000685871.1:c.1431T>C	ENSP00000509964.1:p.Ile477=
ENST00000686159.1:n.1470T>C
ENST00000686486.1:n.439T>C
ENST00000687302.1:n.1517T>C
ENST00000687357.1:c.1431T>C	ENSP00000509549.1:p.Ile477=
ENST00000687625.1:n.586T>C
ENST00000687787.1:c.1431T>C	ENSP00000509440.1:p.Ile477=
ENST00000688201.1:n.1463T>C
ENST00000688226.1:n.1363T>C
ENST00000688869.1:n.1737T>C
ENST00000689788.1:c.1225T>C	ENSP00000508973.1:n.1225T>C
ENST00000689898.1:c.1435T>C	ENSP00000509651.1:p.Phe479Leu
ENST00000690070.1:c.1431T>C	ENSP00000509654.1:p.Ile477=
ENST00000690267.1:c.1295T>C	ENSP00000510432.1:n.1295T>C
ENST00000690552.1:n.1292T>C
ENST00000691138.1:n.1292T>C
ENST00000691969.1:c.1006T>C	ENSP00000510244.1:n.1006T>C
ENST00000692232.1:n.2587T>C
ENST00000692233.1:c.1295T>C	ENSP00000509698.1:n.1295T>C
ENST00000692380.1:n.586T>C
ENST00000692447.1:n.2547T>C
ENST00000693094.1:c.1431T>C	ENSP00000510161.1:p.Ile477=
ENST00000342694.7:c.1431T>C MANE Select	ENSP00000341083.2:p.Ile477=
ENST00000342694.6:c.1431T>C	ENSP00000341083.2:p.Ile477=
ENST00000464810.5:n.1431T>C
NM_003995.3:c.1431T>C	NP_003986.2:p.Ile477=
XM_005251478.3:c.1431T>C	XP_005251535.1:p.Ile477=
XM_005251479.3:c.444T>C	XP_005251536.1:p.Ile148=
XM_006716778.2:c.1431T>C	XP_006716841.1:p.Ile477=
XM_011517889.1:c.444T>C	XP_011516191.1:p.Ile148=
XM_011517890.1:c.444T>C	XP_011516192.1:p.Ile148=
XM_011517891.1:c.444T>C	XP_011516193.1:p.Ile148=
XM_011517892.1:c.444T>C	XP_011516194.1:p.Ile148=
XM_011517893.1:c.444T>C	XP_011516195.1:p.Ile148=
XM_011517894.1:c.444T>C	XP_011516196.1:p.Ile148=
XM_011517895.1:c.27T>C	XP_011516197.1:p.Ile9=
XM_024447556.1:c.1431T>C	XP_024303324.1:p.Ile477=
XM_024447557.1:c.1431T>C	XP_024303325.1:p.Ile477=
XM_024447558.1:c.444T>C	XP_024303326.1:p.Ile148=
XM_024447559.1:c.27T>C	XP_024303327.1:p.Ile9=
XM_024447560.1:c.27T>C	XP_024303328.1:p.Ile9=
XM_024447561.1:c.27T>C	XP_024303329.1:p.Ile9=
NM_003995.4:c.1431T>C MANE Select	NP_003986.2:p.Ile477=
NM_001378923.1:c.1431T>C	NP_001365852.1:p.Ile477=