Canonical Allele Identifier: CA2429868886
Gene: HUWE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.53534021A= , CM000685.2:g.53534021A= GRCh38
NC_000023.10:g.53560982A= , CM000685.1:g.53560982A= GRCh37
NC_000023.9:g.53577707A= NCBI36
NG_016261.2:g.157713T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000704099.1:c.12792T= ENSP00000515693.1:p.Pro4264=
ENST00000262854.11:c.13008T= MANE Select ENSP00000262854.6:p.Pro4336=
ENST00000262854.10:c.13008T= ENSP00000262854.6:p.Pro4336=
ENST00000342160.7:c.13008T= ENSP00000340648.3:p.Pro4336=
ENST00000426907.5:c.3475T=
ENST00000488459.1:n.321T=
ENST00000612484.4:c.12981T= ENSP00000479451.1:p.Pro4327=
NM_031407.6:c.13008T= NP_113584.3:p.Pro4336=
XM_005261965.2:c.13008T= XP_005262022.1:p.Pro4336=
XM_011530746.1:c.13257T= XP_011529048.1:p.Pro4419=
XM_011530747.1:c.13257T= XP_011529049.1:p.Pro4419=
XM_011530748.1:c.13257T= XP_011529050.1:p.Pro4419=
XM_011530749.1:c.13257T= XP_011529051.1:p.Pro4419=
XM_011530750.1:c.13257T= XP_011529052.1:p.Pro4419=
XM_011530751.1:c.13257T= XP_011529053.1:p.Pro4419=
XM_011530752.1:c.13254T= XP_011529054.1:p.Pro4418=
XM_011530753.1:c.13212T= XP_011529055.1:p.Pro4404=
XM_011530754.1:c.13209T= XP_011529056.1:p.Pro4403=
XM_011530755.1:c.13206T= XP_011529057.1:p.Pro4402=
XM_011530756.1:c.13158T= XP_011529058.1:p.Pro4386=
XM_011530757.1:c.12855T= XP_011529059.1:p.Pro4285=
XM_005261965.4:c.13008T= XP_005262022.1:p.Pro4336=
XM_011530751.2:c.13257T= XP_011529053.1:p.Pro4419=
XM_017029191.1:c.13389T= XP_016884680.1:p.Pro4463=
XM_017029192.1:c.13386T= XP_016884681.1:p.Pro4462=
XM_017029193.1:c.13368T= XP_016884682.1:p.Pro4456=
XM_017029194.1:c.13344T= XP_016884683.1:p.Pro4448=
XM_017029195.1:c.13341T= XP_016884684.1:p.Pro4447=
XM_017029196.1:c.13338T= XP_016884685.1:p.Pro4446=
XM_017029197.1:c.13290T= XP_016884686.1:p.Pro4430=
XM_017029198.2:c.13278T= XP_016884687.1:p.Pro4426=
XM_017029199.1:c.13278T= XP_016884688.1:p.Pro4426=
XM_017029200.1:c.13278T= XP_016884689.1:p.Pro4426=
XM_017029201.1:c.13278T= XP_016884690.1:p.Pro4426=
XM_017029202.1:c.13278T= XP_016884691.1:p.Pro4426=
XM_017029203.1:c.13278T= XP_016884692.1:p.Pro4426=
XM_017029204.1:c.13140T= XP_016884693.1:p.Pro4380=
XM_017029206.1:c.12987T= XP_016884695.1:p.Pro4329=
XM_024452322.1:c.13257T= XP_024308090.1:p.Pro4419=
NM_031407.7:c.13008T= MANE Select NP_113584.3:p.Pro4336=