Canonical Allele Identifier: CA2429870454
Gene: HUWE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.53537579G= , CM000685.2:g.53537579G= GRCh38
NC_000023.10:g.53564540G= , CM000685.1:g.53564540G= GRCh37
NC_000023.9:g.53581265G= NCBI36
NG_016261.2:g.154155C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000704099.1:c.11898C= ENSP00000515693.1:p.Ser3966=
ENST00000262854.11:c.12114C= MANE Select ENSP00000262854.6:p.Ser4038=
ENST00000262854.10:c.12114C= ENSP00000262854.6:p.Ser4038=
ENST00000342160.7:c.12114C= ENSP00000340648.3:p.Ser4038=
ENST00000426907.5:c.2581C=
ENST00000480438.1:n.249C=
ENST00000612484.4:c.12087C= ENSP00000479451.1:p.Ser4029=
NM_031407.6:c.12114C= NP_113584.3:p.Ser4038=
XM_005261965.2:c.12114C= XP_005262022.1:p.Ser4038=
XM_011530746.1:c.12363C= XP_011529048.1:p.Ser4121=
XM_011530747.1:c.12363C= XP_011529049.1:p.Ser4121=
XM_011530748.1:c.12363C= XP_011529050.1:p.Ser4121=
XM_011530749.1:c.12363C= XP_011529051.1:p.Ser4121=
XM_011530750.1:c.12363C= XP_011529052.1:p.Ser4121=
XM_011530751.1:c.12363C= XP_011529053.1:p.Ser4121=
XM_011530752.1:c.12360C= XP_011529054.1:p.Ser4120=
XM_011530753.1:c.12318C= XP_011529055.1:p.Ser4106=
XM_011530754.1:c.12315C= XP_011529056.1:p.Ser4105=
XM_011530755.1:c.12312C= XP_011529057.1:p.Ser4104=
XM_011530756.1:c.12264C= XP_011529058.1:p.Ser4088=
XM_011530757.1:c.11961C= XP_011529059.1:p.Ser3987=
XM_005261965.4:c.12114C= XP_005262022.1:p.Ser4038=
XM_011530751.2:c.12363C= XP_011529053.1:p.Ser4121=
XM_017029191.1:c.12495C= XP_016884680.1:p.Ser4165=
XM_017029192.1:c.12492C= XP_016884681.1:p.Ser4164=
XM_017029193.1:c.12474C= XP_016884682.1:p.Ser4158=
XM_017029194.1:c.12450C= XP_016884683.1:p.Ser4150=
XM_017029195.1:c.12447C= XP_016884684.1:p.Ser4149=
XM_017029196.1:c.12444C= XP_016884685.1:p.Ser4148=
XM_017029197.1:c.12396C= XP_016884686.1:p.Ser4132=
XM_017029198.2:c.12384C= XP_016884687.1:p.Ser4128=
XM_017029199.1:c.12384C= XP_016884688.1:p.Ser4128=
XM_017029200.1:c.12384C= XP_016884689.1:p.Ser4128=
XM_017029201.1:c.12384C= XP_016884690.1:p.Ser4128=
XM_017029202.1:c.12384C= XP_016884691.1:p.Ser4128=
XM_017029203.1:c.12384C= XP_016884692.1:p.Ser4128=
XM_017029204.1:c.12246C= XP_016884693.1:p.Ser4082=
XM_017029206.1:c.12093C= XP_016884695.1:p.Ser4031=
XM_024452322.1:c.12363C= XP_024308090.1:p.Ser4121=
NM_031407.7:c.12114C= MANE Select NP_113584.3:p.Ser4038=