Canonical Allele Identifier: CA464615622

Gene: NPR2

Linked Data

• gnomAD v4: 9-35806132-G-A
• MyVariant Identifiers: chr9:g.35806129G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35806132G>A , CM000671.2:g.35806132G>A	GRCh38
NC_000009.11:g.35806129G>A , CM000671.1:g.35806129G>A	GRCh37
NC_000009.10:g.35796129G>A	NCBI36
NG_009249.1:g.18724G>A
NG_047141.1:g.11141C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421267.6:c.311G>A
ENST00000448821.6:c.2271G>A	ENSP00000402902.2:p.Leu757=
ENST00000685871.1:c.2199G>A	ENSP00000509964.1:p.Leu733=
ENST00000686159.1:n.2310G>A
ENST00000686486.1:n.1441G>A
ENST00000687302.1:n.2385G>A
ENST00000687357.1:c.2124G>A	ENSP00000509549.1:p.Leu708=
ENST00000687625.1:n.1426G>A
ENST00000687787.1:c.2430G>A	ENSP00000509440.1:p.Leu810=
ENST00000688201.1:n.2228G>A
ENST00000688226.1:n.2203G>A
ENST00000688869.1:n.2577G>A
ENST00000689788.1:c.2065G>A	ENSP00000508973.1:n.2065G>A
ENST00000689898.1:c.2128G>A	ENSP00000509651.1:n.2128G>A
ENST00000690070.1:c.2355G>A	ENSP00000509654.1:p.Leu785=
ENST00000690267.1:c.2060G>A	ENSP00000510432.1:n.2060G>A
ENST00000690552.1:n.2132G>A
ENST00000691138.1:n.2060G>A
ENST00000691969.1:c.1771G>A	ENSP00000510244.1:n.1771G>A
ENST00000692232.1:n.3586G>A
ENST00000692233.1:c.2135G>A	ENSP00000509698.1:n.2135G>A
ENST00000692380.1:n.1426G>A
ENST00000692447.1:n.3387G>A
ENST00000693094.1:c.2271G>A	ENSP00000510161.1:p.Leu757=
ENST00000342694.7:c.2271G>A MANE Select	ENSP00000341083.2:p.Leu757=
ENST00000342694.6:c.2271G>A	ENSP00000341083.2:p.Leu757=
ENST00000421267.5:c.311G>A
ENST00000447210.5:c.48G>A	ENSP00000393029.1:p.Leu16=
ENST00000464810.5:n.2271G>A
NM_003995.3:c.2271G>A	NP_003986.2:p.Leu757=
XM_005251478.3:c.2280G>A	XP_005251535.1:p.Leu760=
XM_005251479.3:c.1293G>A	XP_005251536.1:p.Leu431=
XM_006716778.2:c.2208G>A	XP_006716841.1:p.Leu736=
XM_011517889.1:c.1293G>A	XP_011516191.1:p.Leu431=
XM_011517890.1:c.1293G>A	XP_011516192.1:p.Leu431=
XM_011517891.1:c.1293G>A	XP_011516193.1:p.Leu431=
XM_011517892.1:c.1293G>A	XP_011516194.1:p.Leu431=
XM_011517893.1:c.1293G>A	XP_011516195.1:p.Leu431=
XM_011517894.1:c.1293G>A	XP_011516196.1:p.Leu431=
XM_011517895.1:c.876G>A	XP_011516197.1:p.Leu292=
XM_024447556.1:c.2439G>A	XP_024303324.1:p.Leu813=
XM_024447557.1:c.2430G>A	XP_024303325.1:p.Leu810=
XM_024447558.1:c.1452G>A	XP_024303326.1:p.Leu484=
XM_024447559.1:c.1035G>A	XP_024303327.1:p.Leu345=
XM_024447560.1:c.1026G>A	XP_024303328.1:p.Leu342=
XM_024447561.1:c.867G>A	XP_024303329.1:p.Leu289=
NM_003995.4:c.2271G>A MANE Select	NP_003986.2:p.Leu757=
NM_001378923.1:c.2280G>A	NP_001365852.1:p.Leu760=