Canonical Allele Identifier: CA1846144567
Community Standard Title: NM_003995.4(NPR2):c.1963C= (p.Arg655=)
Gene: NPR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.35805586C= , CM000671.2:g.35805586C= GRCh38
NC_000009.11:g.35805583C= , CM000671.1:g.35805583C= GRCh37
NC_000009.10:g.35795583C= NCBI36
NG_009249.1:g.18178C=

Transcript Alleles

HGVS Amino-acid Change
NM_003995.4:c.1963C= MANE Select NP_003986.2:p.Arg655=
ENST00000342694.7:c.1963C= MANE Select ENSP00000341083.2:p.Arg655=
NM_001378923.1:c.1972C= NP_001365852.1:p.Arg658=
NM_003995.3:c.1963C= NP_003986.2:p.Arg655=
ENST00000342694.6:c.1963C= ENSP00000341083.2:p.Arg655=
ENST00000421267.5:c.57C=
ENST00000421267.6:c.57C=
ENST00000448821.6:c.1963C= ENSP00000402902.2:p.Arg655=
ENST00000464810.5:n.1963C=
ENST00000685871.1:c.1891C= ENSP00000509964.1:p.Arg631=
ENST00000686159.1:n.2002C=
ENST00000686486.1:n.1133C=
ENST00000687302.1:n.2077C=
ENST00000687357.1:c.1816C= ENSP00000509549.1:p.Arg606=
ENST00000687625.1:n.1118C=
ENST00000687787.1:c.1963C= ENSP00000509440.1:p.Arg655=
ENST00000688201.1:n.1920C=
ENST00000688226.1:n.1895C=
ENST00000688869.1:n.2269C=
ENST00000689788.1:c.1757C= ENSP00000508973.1:n.1757C=
ENST00000689898.1:c.1820C= ENSP00000509651.1:n.1820C=
ENST00000690070.1:c.1888C= ENSP00000509654.1:p.Arg630=
ENST00000690267.1:c.1752C= ENSP00000510432.1:n.1752C=
ENST00000690552.1:n.1824C=
ENST00000691138.1:n.1752C=
ENST00000691969.1:c.1463C= ENSP00000510244.1:n.1463C=
ENST00000692232.1:n.3119C=
ENST00000692233.1:c.1827C= ENSP00000509698.1:n.1827C=
ENST00000692380.1:n.1118C=
ENST00000692447.1:n.3079C=
ENST00000693094.1:c.1963C= ENSP00000510161.1:p.Arg655=
XM_005251478.3:c.1972C= XP_005251535.1:p.Arg658=
XM_005251479.3:c.985C= XP_005251536.1:p.Arg329=
XM_006716778.2:c.1900C= XP_006716841.1:p.Arg634=
XM_011517889.1:c.985C= XP_011516191.1:p.Arg329=
XM_011517890.1:c.985C= XP_011516192.1:p.Arg329=
XM_011517891.1:c.985C= XP_011516193.1:p.Arg329=
XM_011517892.1:c.985C= XP_011516194.1:p.Arg329=
XM_011517893.1:c.985C= XP_011516195.1:p.Arg329=
XM_011517894.1:c.985C= XP_011516196.1:p.Arg329=
XM_011517895.1:c.568C= XP_011516197.1:p.Arg190=
XM_024447556.1:c.1972C= XP_024303324.1:p.Arg658=
XM_024447557.1:c.1963C= XP_024303325.1:p.Arg655=
XM_024447558.1:c.985C= XP_024303326.1:p.Arg329=
XM_024447559.1:c.568C= XP_024303327.1:p.Arg190=
XM_024447560.1:c.559C= XP_024303328.1:p.Arg187=
XM_024447561.1:c.559C= XP_024303329.1:p.Arg187=