Canonical Allele Identifier: CA2429868925
Gene: HUWE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.53534169G= , CM000685.2:g.53534169G= GRCh38
NC_000023.10:g.53561130G= , CM000685.1:g.53561130G= GRCh37
NC_000023.9:g.53577855G= NCBI36
NG_016261.2:g.157565C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000704099.1:c.12644C= ENSP00000515693.1:p.Ser4215=
ENST00000262854.11:c.12860C= MANE Select ENSP00000262854.6:p.Ser4287=
ENST00000262854.10:c.12860C= ENSP00000262854.6:p.Ser4287=
ENST00000342160.7:c.12860C= ENSP00000340648.3:p.Ser4287=
ENST00000426907.5:c.3327C=
ENST00000488459.1:n.173C=
ENST00000612484.4:c.12833C= ENSP00000479451.1:p.Ser4278=
NM_031407.6:c.12860C= NP_113584.3:p.Ser4287=
XM_005261965.2:c.12860C= XP_005262022.1:p.Ser4287=
XM_011530746.1:c.13109C= XP_011529048.1:p.Ser4370=
XM_011530747.1:c.13109C= XP_011529049.1:p.Ser4370=
XM_011530748.1:c.13109C= XP_011529050.1:p.Ser4370=
XM_011530749.1:c.13109C= XP_011529051.1:p.Ser4370=
XM_011530750.1:c.13109C= XP_011529052.1:p.Ser4370=
XM_011530751.1:c.13109C= XP_011529053.1:p.Ser4370=
XM_011530752.1:c.13106C= XP_011529054.1:p.Ser4369=
XM_011530753.1:c.13064C= XP_011529055.1:p.Ser4355=
XM_011530754.1:c.13061C= XP_011529056.1:p.Ser4354=
XM_011530755.1:c.13058C= XP_011529057.1:p.Ser4353=
XM_011530756.1:c.13010C= XP_011529058.1:p.Ser4337=
XM_011530757.1:c.12707C= XP_011529059.1:p.Ser4236=
XM_005261965.4:c.12860C= XP_005262022.1:p.Ser4287=
XM_011530751.2:c.13109C= XP_011529053.1:p.Ser4370=
XM_017029191.1:c.13241C= XP_016884680.1:p.Ser4414=
XM_017029192.1:c.13238C= XP_016884681.1:p.Ser4413=
XM_017029193.1:c.13220C= XP_016884682.1:p.Ser4407=
XM_017029194.1:c.13196C= XP_016884683.1:p.Ser4399=
XM_017029195.1:c.13193C= XP_016884684.1:p.Ser4398=
XM_017029196.1:c.13190C= XP_016884685.1:p.Ser4397=
XM_017029197.1:c.13142C= XP_016884686.1:p.Ser4381=
XM_017029198.2:c.13130C= XP_016884687.1:p.Ser4377=
XM_017029199.1:c.13130C= XP_016884688.1:p.Ser4377=
XM_017029200.1:c.13130C= XP_016884689.1:p.Ser4377=
XM_017029201.1:c.13130C= XP_016884690.1:p.Ser4377=
XM_017029202.1:c.13130C= XP_016884691.1:p.Ser4377=
XM_017029203.1:c.13130C= XP_016884692.1:p.Ser4377=
XM_017029204.1:c.12992C= XP_016884693.1:p.Ser4331=
XM_017029206.1:c.12839C= XP_016884695.1:p.Ser4280=
XM_024452322.1:c.13109C= XP_024308090.1:p.Ser4370=
NM_031407.7:c.12860C= MANE Select NP_113584.3:p.Ser4287=