Canonical Allele Identifier: CA2429868913
Gene: HUWE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.53534125C= , CM000685.2:g.53534125C= GRCh38
NC_000023.10:g.53561086C= , CM000685.1:g.53561086C= GRCh37
NC_000023.9:g.53577811C= NCBI36
NG_016261.2:g.157609G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000704099.1:c.12688G= ENSP00000515693.1:p.Gly4230=
ENST00000262854.11:c.12904G= MANE Select ENSP00000262854.6:p.Gly4302=
ENST00000262854.10:c.12904G= ENSP00000262854.6:p.Gly4302=
ENST00000342160.7:c.12904G= ENSP00000340648.3:p.Gly4302=
ENST00000426907.5:c.3371G=
ENST00000488459.1:n.217G=
ENST00000612484.4:c.12877G= ENSP00000479451.1:p.Gly4293=
NM_031407.6:c.12904G= NP_113584.3:p.Gly4302=
XM_005261965.2:c.12904G= XP_005262022.1:p.Gly4302=
XM_011530746.1:c.13153G= XP_011529048.1:p.Gly4385=
XM_011530747.1:c.13153G= XP_011529049.1:p.Gly4385=
XM_011530748.1:c.13153G= XP_011529050.1:p.Gly4385=
XM_011530749.1:c.13153G= XP_011529051.1:p.Gly4385=
XM_011530750.1:c.13153G= XP_011529052.1:p.Gly4385=
XM_011530751.1:c.13153G= XP_011529053.1:p.Gly4385=
XM_011530752.1:c.13150G= XP_011529054.1:p.Gly4384=
XM_011530753.1:c.13108G= XP_011529055.1:p.Gly4370=
XM_011530754.1:c.13105G= XP_011529056.1:p.Gly4369=
XM_011530755.1:c.13102G= XP_011529057.1:p.Gly4368=
XM_011530756.1:c.13054G= XP_011529058.1:p.Gly4352=
XM_011530757.1:c.12751G= XP_011529059.1:p.Gly4251=
XM_005261965.4:c.12904G= XP_005262022.1:p.Gly4302=
XM_011530751.2:c.13153G= XP_011529053.1:p.Gly4385=
XM_017029191.1:c.13285G= XP_016884680.1:p.Gly4429=
XM_017029192.1:c.13282G= XP_016884681.1:p.Gly4428=
XM_017029193.1:c.13264G= XP_016884682.1:p.Gly4422=
XM_017029194.1:c.13240G= XP_016884683.1:p.Gly4414=
XM_017029195.1:c.13237G= XP_016884684.1:p.Gly4413=
XM_017029196.1:c.13234G= XP_016884685.1:p.Gly4412=
XM_017029197.1:c.13186G= XP_016884686.1:p.Gly4396=
XM_017029198.2:c.13174G= XP_016884687.1:p.Gly4392=
XM_017029199.1:c.13174G= XP_016884688.1:p.Gly4392=
XM_017029200.1:c.13174G= XP_016884689.1:p.Gly4392=
XM_017029201.1:c.13174G= XP_016884690.1:p.Gly4392=
XM_017029202.1:c.13174G= XP_016884691.1:p.Gly4392=
XM_017029203.1:c.13174G= XP_016884692.1:p.Gly4392=
XM_017029204.1:c.13036G= XP_016884693.1:p.Gly4346=
XM_017029206.1:c.12883G= XP_016884695.1:p.Gly4295=
XM_024452322.1:c.13153G= XP_024308090.1:p.Gly4385=
NM_031407.7:c.12904G= MANE Select NP_113584.3:p.Gly4302=