Canonical Allele Identifier: CA1846149708
Community Standard Title: NM_003995.4(NPR2):c.2647G= (p.Val883=)
Gene: NPR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.35807333G= , CM000671.2:g.35807333G= GRCh38
NC_000009.11:g.35807330G= , CM000671.1:g.35807330G= GRCh37
NC_000009.10:g.35797330G= NCBI36
NG_009249.1:g.19925G=
NG_047141.1:g.9940C=

Transcript Alleles

HGVS Amino-acid Change
NM_003995.4:c.2647G= MANE Select NP_003986.2:p.Val883=
ENST00000342694.7:c.2647G= MANE Select ENSP00000341083.2:p.Val883=
NM_001378923.1:c.2656G= NP_001365852.1:p.Val886=
NM_003995.3:c.2647G= NP_003986.2:p.Val883=
ENST00000342694.6:c.2647G= ENSP00000341083.2:p.Val883=
ENST00000421267.5:c.687G=
ENST00000421267.6:c.687G=
ENST00000447210.5:c.424G= ENSP00000393029.1:p.Val142=
ENST00000448821.5:c.134G=
ENST00000448821.6:c.2647G= ENSP00000402902.2:p.Val883=
ENST00000464810.5:n.2647G=
ENST00000685871.1:c.2575G= ENSP00000509964.1:p.Val859=
ENST00000686159.1:n.2686G=
ENST00000686486.1:n.1817G=
ENST00000687302.1:n.2761G=
ENST00000687357.1:c.2500G= ENSP00000509549.1:p.Val834=
ENST00000687625.1:n.1802G=
ENST00000687787.1:c.2806G= ENSP00000509440.1:p.Val936=
ENST00000688201.1:n.2604G=
ENST00000688226.1:n.2579G=
ENST00000688869.1:n.2953G=
ENST00000689788.1:c.2441G= ENSP00000508973.1:n.2441G=
ENST00000689898.1:c.2504G= ENSP00000509651.1:n.2504G=
ENST00000690070.1:c.2731G= ENSP00000509654.1:p.Val911=
ENST00000690267.1:c.2436G= ENSP00000510432.1:n.2436G=
ENST00000690552.1:n.2992G=
ENST00000691138.1:n.2920G=
ENST00000691969.1:c.2147G= ENSP00000510244.1:n.2147G=
ENST00000692232.1:n.3962G=
ENST00000692233.1:c.2511G= ENSP00000509698.1:n.2511G=
ENST00000692380.1:n.1802G=
ENST00000692447.1:n.3763G=
ENST00000693094.1:c.2737G= ENSP00000510161.1:p.Val913=
XM_005251478.3:c.2656G= XP_005251535.1:p.Val886=
XM_005251479.3:c.1669G= XP_005251536.1:p.Val557=
XM_006716778.2:c.2584G= XP_006716841.1:p.Val862=
XM_011517889.1:c.1669G= XP_011516191.1:p.Val557=
XM_011517890.1:c.1669G= XP_011516192.1:p.Val557=
XM_011517891.1:c.1669G= XP_011516193.1:p.Val557=
XM_011517892.1:c.1669G= XP_011516194.1:p.Val557=
XM_011517893.1:c.1669G= XP_011516195.1:p.Val557=
XM_011517894.1:c.1669G= XP_011516196.1:p.Val557=
XM_011517895.1:c.1252G= XP_011516197.1:p.Val418=
XM_024447556.1:c.2815G= XP_024303324.1:p.Val939=
XM_024447557.1:c.2806G= XP_024303325.1:p.Val936=
XM_024447558.1:c.1828G= XP_024303326.1:p.Val610=
XM_024447559.1:c.1411G= XP_024303327.1:p.Val471=
XM_024447560.1:c.1402G= XP_024303328.1:p.Val468=
XM_024447561.1:c.1243G= XP_024303329.1:p.Val415=