Canonical Allele Identifier: CA2429869117
Gene: HUWE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.53534637C= , CM000685.2:g.53534637C= GRCh38
NC_000023.10:g.53561598C= , CM000685.1:g.53561598C= GRCh37
NC_000023.9:g.53578323C= NCBI36
NG_016261.2:g.157097G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000704099.1:c.12494G= ENSP00000515693.1:p.Arg4165=
ENST00000262854.11:c.12710G= MANE Select ENSP00000262854.6:p.Arg4237=
ENST00000262854.10:c.12710G= ENSP00000262854.6:p.Arg4237=
ENST00000342160.7:c.12710G= ENSP00000340648.3:p.Arg4237=
ENST00000426907.5:c.3177G=
ENST00000488459.1:n.23G=
ENST00000612484.4:c.12683G= ENSP00000479451.1:p.Arg4228=
NM_031407.6:c.12710G= NP_113584.3:p.Arg4237=
XM_005261965.2:c.12710G= XP_005262022.1:p.Arg4237=
XM_011530746.1:c.12959G= XP_011529048.1:p.Arg4320=
XM_011530747.1:c.12959G= XP_011529049.1:p.Arg4320=
XM_011530748.1:c.12959G= XP_011529050.1:p.Arg4320=
XM_011530749.1:c.12959G= XP_011529051.1:p.Arg4320=
XM_011530750.1:c.12959G= XP_011529052.1:p.Arg4320=
XM_011530751.1:c.12959G= XP_011529053.1:p.Arg4320=
XM_011530752.1:c.12956G= XP_011529054.1:p.Arg4319=
XM_011530753.1:c.12914G= XP_011529055.1:p.Arg4305=
XM_011530754.1:c.12911G= XP_011529056.1:p.Arg4304=
XM_011530755.1:c.12908G= XP_011529057.1:p.Arg4303=
XM_011530756.1:c.12860G= XP_011529058.1:p.Arg4287=
XM_011530757.1:c.12557G= XP_011529059.1:p.Arg4186=
XM_005261965.4:c.12710G= XP_005262022.1:p.Arg4237=
XM_011530751.2:c.12959G= XP_011529053.1:p.Arg4320=
XM_017029191.1:c.13091G= XP_016884680.1:p.Arg4364=
XM_017029192.1:c.13088G= XP_016884681.1:p.Arg4363=
XM_017029193.1:c.13070G= XP_016884682.1:p.Arg4357=
XM_017029194.1:c.13046G= XP_016884683.1:p.Arg4349=
XM_017029195.1:c.13043G= XP_016884684.1:p.Arg4348=
XM_017029196.1:c.13040G= XP_016884685.1:p.Arg4347=
XM_017029197.1:c.12992G= XP_016884686.1:p.Arg4331=
XM_017029198.2:c.12980G= XP_016884687.1:p.Arg4327=
XM_017029199.1:c.12980G= XP_016884688.1:p.Arg4327=
XM_017029200.1:c.12980G= XP_016884689.1:p.Arg4327=
XM_017029201.1:c.12980G= XP_016884690.1:p.Arg4327=
XM_017029202.1:c.12980G= XP_016884691.1:p.Arg4327=
XM_017029203.1:c.12980G= XP_016884692.1:p.Arg4327=
XM_017029204.1:c.12842G= XP_016884693.1:p.Arg4281=
XM_017029206.1:c.12689G= XP_016884695.1:p.Arg4230=
XM_024452322.1:c.12959G= XP_024308090.1:p.Arg4320=
NM_031407.7:c.12710G= MANE Select NP_113584.3:p.Arg4237=