Canonical Allele Identifier: CA464465003

Gene: NPR2

Linked Data

• MyVariant Identifiers: chr9:g.35806189A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35806192A>C , CM000671.2:g.35806192A>C	GRCh38
NC_000009.11:g.35806189A>C , CM000671.1:g.35806189A>C	GRCh37
NC_000009.10:g.35796189A>C	NCBI36
NG_009249.1:g.18784A>C
NG_047141.1:g.11081T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421267.6:c.371A>C
ENST00000448821.6:c.2331A>C	ENSP00000402902.2:p.Pro777=
ENST00000685871.1:c.2259A>C	ENSP00000509964.1:p.Pro753=
ENST00000686159.1:n.2370A>C
ENST00000686486.1:n.1501A>C
ENST00000687302.1:n.2445A>C
ENST00000687357.1:c.2184A>C	ENSP00000509549.1:p.Pro728=
ENST00000687625.1:n.1486A>C
ENST00000687787.1:c.2490A>C	ENSP00000509440.1:p.Pro830=
ENST00000688201.1:n.2288A>C
ENST00000688226.1:n.2263A>C
ENST00000688869.1:n.2637A>C
ENST00000689788.1:c.2125A>C	ENSP00000508973.1:n.2125A>C
ENST00000689898.1:c.2188A>C	ENSP00000509651.1:n.2188A>C
ENST00000690070.1:c.2415A>C	ENSP00000509654.1:p.Pro805=
ENST00000690267.1:c.2120A>C	ENSP00000510432.1:n.2120A>C
ENST00000690552.1:n.2192A>C
ENST00000691138.1:n.2120A>C
ENST00000691969.1:c.1831A>C	ENSP00000510244.1:n.1831A>C
ENST00000692232.1:n.3646A>C
ENST00000692233.1:c.2195A>C	ENSP00000509698.1:n.2195A>C
ENST00000692380.1:n.1486A>C
ENST00000692447.1:n.3447A>C
ENST00000693094.1:c.2331A>C	ENSP00000510161.1:p.Pro777=
ENST00000342694.7:c.2331A>C MANE Select	ENSP00000341083.2:p.Pro777=
ENST00000342694.6:c.2331A>C	ENSP00000341083.2:p.Pro777=
ENST00000421267.5:c.371A>C
ENST00000447210.5:c.108A>C	ENSP00000393029.1:p.Pro36=
ENST00000464810.5:n.2331A>C
NM_003995.3:c.2331A>C	NP_003986.2:p.Pro777=
XM_005251478.3:c.2340A>C	XP_005251535.1:p.Pro780=
XM_005251479.3:c.1353A>C	XP_005251536.1:p.Pro451=
XM_006716778.2:c.2268A>C	XP_006716841.1:p.Pro756=
XM_011517889.1:c.1353A>C	XP_011516191.1:p.Pro451=
XM_011517890.1:c.1353A>C	XP_011516192.1:p.Pro451=
XM_011517891.1:c.1353A>C	XP_011516193.1:p.Pro451=
XM_011517892.1:c.1353A>C	XP_011516194.1:p.Pro451=
XM_011517893.1:c.1353A>C	XP_011516195.1:p.Pro451=
XM_011517894.1:c.1353A>C	XP_011516196.1:p.Pro451=
XM_011517895.1:c.936A>C	XP_011516197.1:p.Pro312=
XM_024447556.1:c.2499A>C	XP_024303324.1:p.Pro833=
XM_024447557.1:c.2490A>C	XP_024303325.1:p.Pro830=
XM_024447558.1:c.1512A>C	XP_024303326.1:p.Pro504=
XM_024447559.1:c.1095A>C	XP_024303327.1:p.Pro365=
XM_024447560.1:c.1086A>C	XP_024303328.1:p.Pro362=
XM_024447561.1:c.927A>C	XP_024303329.1:p.Pro309=
NM_003995.4:c.2331A>C MANE Select	NP_003986.2:p.Pro777=
NM_001378923.1:c.2340A>C	NP_001365852.1:p.Pro780=