Canonical Allele Identifier: CA373379242

Gene: NPR2

Linked Data

• MyVariant Identifiers: chr9:g.35806181G>C (hg19) ; chr9:g.35806184G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35806184G>C , CM000671.2:g.35806184G>C	GRCh38
NC_000009.11:g.35806181G>C , CM000671.1:g.35806181G>C	GRCh37
NC_000009.10:g.35796181G>C	NCBI36
NG_009249.1:g.18776G>C
NG_047141.1:g.11089C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421267.6:c.363G>C
ENST00000448821.6:c.2323G>C	ENSP00000402902.2:p.Glu775Gln
ENST00000685871.1:c.2251G>C	ENSP00000509964.1:p.Glu751Gln
ENST00000686159.1:n.2362G>C
ENST00000686486.1:n.1493G>C
ENST00000687302.1:n.2437G>C
ENST00000687357.1:c.2176G>C	ENSP00000509549.1:p.Glu726Gln
ENST00000687625.1:n.1478G>C
ENST00000687787.1:c.2482G>C	ENSP00000509440.1:p.Glu828Gln
ENST00000688201.1:n.2280G>C
ENST00000688226.1:n.2255G>C
ENST00000688869.1:n.2629G>C
ENST00000689788.1:c.2117G>C	ENSP00000508973.1:n.2117G>C
ENST00000689898.1:c.2180G>C	ENSP00000509651.1:n.2180G>C
ENST00000690070.1:c.2407G>C	ENSP00000509654.1:p.Glu803Gln
ENST00000690267.1:c.2112G>C	ENSP00000510432.1:n.2112G>C
ENST00000690552.1:n.2184G>C
ENST00000691138.1:n.2112G>C
ENST00000691969.1:c.1823G>C	ENSP00000510244.1:n.1823G>C
ENST00000692232.1:n.3638G>C
ENST00000692233.1:c.2187G>C	ENSP00000509698.1:n.2187G>C
ENST00000692380.1:n.1478G>C
ENST00000692447.1:n.3439G>C
ENST00000693094.1:c.2323G>C	ENSP00000510161.1:p.Glu775Gln
ENST00000342694.7:c.2323G>C MANE Select	ENSP00000341083.2:p.Glu775Gln
ENST00000342694.6:c.2323G>C	ENSP00000341083.2:p.Glu775Gln
ENST00000421267.5:c.363G>C
ENST00000447210.5:c.100G>C	ENSP00000393029.1:p.Glu34Gln
ENST00000464810.5:n.2323G>C
NM_003995.3:c.2323G>C	NP_003986.2:p.Glu775Gln
XM_005251478.3:c.2332G>C	XP_005251535.1:p.Glu778Gln
XM_005251479.3:c.1345G>C	XP_005251536.1:p.Glu449Gln
XM_006716778.2:c.2260G>C	XP_006716841.1:p.Glu754Gln
XM_011517889.1:c.1345G>C	XP_011516191.1:p.Glu449Gln
XM_011517890.1:c.1345G>C	XP_011516192.1:p.Glu449Gln
XM_011517891.1:c.1345G>C	XP_011516193.1:p.Glu449Gln
XM_011517892.1:c.1345G>C	XP_011516194.1:p.Glu449Gln
XM_011517893.1:c.1345G>C	XP_011516195.1:p.Glu449Gln
XM_011517894.1:c.1345G>C	XP_011516196.1:p.Glu449Gln
XM_011517895.1:c.928G>C	XP_011516197.1:p.Glu310Gln
XM_024447556.1:c.2491G>C	XP_024303324.1:p.Glu831Gln
XM_024447557.1:c.2482G>C	XP_024303325.1:p.Glu828Gln
XM_024447558.1:c.1504G>C	XP_024303326.1:p.Glu502Gln
XM_024447559.1:c.1087G>C	XP_024303327.1:p.Glu363Gln
XM_024447560.1:c.1078G>C	XP_024303328.1:p.Glu360Gln
XM_024447561.1:c.919G>C	XP_024303329.1:p.Glu307Gln
NM_003995.4:c.2323G>C MANE Select	NP_003986.2:p.Glu775Gln
NM_001378923.1:c.2332G>C	NP_001365852.1:p.Glu778Gln