Canonical Allele Identifier: CA373378950

Gene: NPR2

Linked Data

• gnomAD v4: 9-35806129-A-C
• MyVariant Identifiers: chr9:g.35806126A>C (hg19) ; chr9:g.35806129A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35806129A>C , CM000671.2:g.35806129A>C	GRCh38
NC_000009.11:g.35806126A>C , CM000671.1:g.35806126A>C	GRCh37
NC_000009.10:g.35796126A>C	NCBI36
NG_009249.1:g.18721A>C
NG_047141.1:g.11144T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421267.6:c.308A>C
ENST00000448821.6:c.2268A>C	ENSP00000402902.2:p.Gln756His
ENST00000685871.1:c.2196A>C	ENSP00000509964.1:p.Gln732His
ENST00000686159.1:n.2307A>C
ENST00000686486.1:n.1438A>C
ENST00000687302.1:n.2382A>C
ENST00000687357.1:c.2121A>C	ENSP00000509549.1:p.Gln707His
ENST00000687625.1:n.1423A>C
ENST00000687787.1:c.2427A>C	ENSP00000509440.1:p.Gln809His
ENST00000688201.1:n.2225A>C
ENST00000688226.1:n.2200A>C
ENST00000688869.1:n.2574A>C
ENST00000689788.1:c.2062A>C	ENSP00000508973.1:n.2062A>C
ENST00000689898.1:c.2125A>C	ENSP00000509651.1:n.2125A>C
ENST00000690070.1:c.2352A>C	ENSP00000509654.1:p.Gln784His
ENST00000690267.1:c.2057A>C	ENSP00000510432.1:n.2057A>C
ENST00000690552.1:n.2129A>C
ENST00000691138.1:n.2057A>C
ENST00000691969.1:c.1768A>C	ENSP00000510244.1:n.1768A>C
ENST00000692232.1:n.3583A>C
ENST00000692233.1:c.2132A>C	ENSP00000509698.1:n.2132A>C
ENST00000692380.1:n.1423A>C
ENST00000692447.1:n.3384A>C
ENST00000693094.1:c.2268A>C	ENSP00000510161.1:p.Gln756His
ENST00000342694.7:c.2268A>C MANE Select	ENSP00000341083.2:p.Gln756His
ENST00000342694.6:c.2268A>C	ENSP00000341083.2:p.Gln756His
ENST00000421267.5:c.308A>C
ENST00000447210.5:c.45A>C	ENSP00000393029.1:p.Gln15His
ENST00000464810.5:n.2268A>C
NM_003995.3:c.2268A>C	NP_003986.2:p.Gln756His
XM_005251478.3:c.2277A>C	XP_005251535.1:p.Gln759His
XM_005251479.3:c.1290A>C	XP_005251536.1:p.Gln430His
XM_006716778.2:c.2205A>C	XP_006716841.1:p.Gln735His
XM_011517889.1:c.1290A>C	XP_011516191.1:p.Gln430His
XM_011517890.1:c.1290A>C	XP_011516192.1:p.Gln430His
XM_011517891.1:c.1290A>C	XP_011516193.1:p.Gln430His
XM_011517892.1:c.1290A>C	XP_011516194.1:p.Gln430His
XM_011517893.1:c.1290A>C	XP_011516195.1:p.Gln430His
XM_011517894.1:c.1290A>C	XP_011516196.1:p.Gln430His
XM_011517895.1:c.873A>C	XP_011516197.1:p.Gln291His
XM_024447556.1:c.2436A>C	XP_024303324.1:p.Gln812His
XM_024447557.1:c.2427A>C	XP_024303325.1:p.Gln809His
XM_024447558.1:c.1449A>C	XP_024303326.1:p.Gln483His
XM_024447559.1:c.1032A>C	XP_024303327.1:p.Gln344His
XM_024447560.1:c.1023A>C	XP_024303328.1:p.Gln341His
XM_024447561.1:c.864A>C	XP_024303329.1:p.Gln288His
NM_003995.4:c.2268A>C MANE Select	NP_003986.2:p.Gln756His
NM_001378923.1:c.2277A>C	NP_001365852.1:p.Gln759His