Canonical Allele Identifier: CA373379163

Gene: NPR2

Linked Data

• MyVariant Identifiers: chr9:g.35806165G>A (hg19) ; chr9:g.35806168G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35806168G>A , CM000671.2:g.35806168G>A	GRCh38
NC_000009.11:g.35806165G>A , CM000671.1:g.35806165G>A	GRCh37
NC_000009.10:g.35796165G>A	NCBI36
NG_009249.1:g.18760G>A
NG_047141.1:g.11105C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421267.6:c.347G>A
ENST00000448821.6:c.2307G>A	ENSP00000402902.2:p.Trp769Ter
ENST00000685871.1:c.2235G>A	ENSP00000509964.1:p.Trp745Ter
ENST00000686159.1:n.2346G>A
ENST00000686486.1:n.1477G>A
ENST00000687302.1:n.2421G>A
ENST00000687357.1:c.2160G>A	ENSP00000509549.1:p.Trp720Ter
ENST00000687625.1:n.1462G>A
ENST00000687787.1:c.2466G>A	ENSP00000509440.1:p.Trp822Ter
ENST00000688201.1:n.2264G>A
ENST00000688226.1:n.2239G>A
ENST00000688869.1:n.2613G>A
ENST00000689788.1:c.2101G>A	ENSP00000508973.1:n.2101G>A
ENST00000689898.1:c.2164G>A	ENSP00000509651.1:n.2164G>A
ENST00000690070.1:c.2391G>A	ENSP00000509654.1:p.Trp797Ter
ENST00000690267.1:c.2096G>A	ENSP00000510432.1:n.2096G>A
ENST00000690552.1:n.2168G>A
ENST00000691138.1:n.2096G>A
ENST00000691969.1:c.1807G>A	ENSP00000510244.1:n.1807G>A
ENST00000692232.1:n.3622G>A
ENST00000692233.1:c.2171G>A	ENSP00000509698.1:n.2171G>A
ENST00000692380.1:n.1462G>A
ENST00000692447.1:n.3423G>A
ENST00000693094.1:c.2307G>A	ENSP00000510161.1:p.Trp769Ter
ENST00000342694.7:c.2307G>A MANE Select	ENSP00000341083.2:p.Trp769Ter
ENST00000342694.6:c.2307G>A	ENSP00000341083.2:p.Trp769Ter
ENST00000421267.5:c.347G>A
ENST00000447210.5:c.84G>A	ENSP00000393029.1:p.Trp28Ter
ENST00000464810.5:n.2307G>A
NM_003995.3:c.2307G>A	NP_003986.2:p.Trp769Ter
XM_005251478.3:c.2316G>A	XP_005251535.1:p.Trp772Ter
XM_005251479.3:c.1329G>A	XP_005251536.1:p.Trp443Ter
XM_006716778.2:c.2244G>A	XP_006716841.1:p.Trp748Ter
XM_011517889.1:c.1329G>A	XP_011516191.1:p.Trp443Ter
XM_011517890.1:c.1329G>A	XP_011516192.1:p.Trp443Ter
XM_011517891.1:c.1329G>A	XP_011516193.1:p.Trp443Ter
XM_011517892.1:c.1329G>A	XP_011516194.1:p.Trp443Ter
XM_011517893.1:c.1329G>A	XP_011516195.1:p.Trp443Ter
XM_011517894.1:c.1329G>A	XP_011516196.1:p.Trp443Ter
XM_011517895.1:c.912G>A	XP_011516197.1:p.Trp304Ter
XM_024447556.1:c.2475G>A	XP_024303324.1:p.Trp825Ter
XM_024447557.1:c.2466G>A	XP_024303325.1:p.Trp822Ter
XM_024447558.1:c.1488G>A	XP_024303326.1:p.Trp496Ter
XM_024447559.1:c.1071G>A	XP_024303327.1:p.Trp357Ter
XM_024447560.1:c.1062G>A	XP_024303328.1:p.Trp354Ter
XM_024447561.1:c.903G>A	XP_024303329.1:p.Trp301Ter
NM_003995.4:c.2307G>A MANE Select	NP_003986.2:p.Trp769Ter
NM_001378923.1:c.2316G>A	NP_001365852.1:p.Trp772Ter