Canonical Allele Identifier: CA413163162
Gene: HUWE1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.53568725A>T , CM000685.2:g.53568725A>T GRCh38
NC_000023.10:g.53595685A>T , CM000685.1:g.53595685A>T GRCh37
NC_000023.9:g.53612410A>T NCBI36
NG_016261.2:g.123009T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000704099.1:c.6671T>A ENSP00000515693.1:p.Leu2224Gln
ENST00000262854.11:c.6674T>A MANE Select ENSP00000262854.6:p.Leu2225Gln
ENST00000262854.10:c.6674T>A ENSP00000262854.6:p.Leu2225Gln
ENST00000342160.7:c.6674T>A ENSP00000340648.3:p.Leu2225Gln
ENST00000612484.4:c.6647T>A ENSP00000479451.1:p.Leu2216Gln
NM_031407.6:c.6674T>A NP_113584.3:p.Leu2225Gln
XM_005261965.2:c.6674T>A XP_005262022.1:p.Leu2225Gln
XM_011530746.1:c.6923T>A XP_011529048.1:p.Leu2308Gln
XM_011530747.1:c.6923T>A XP_011529049.1:p.Leu2308Gln
XM_011530748.1:c.6923T>A XP_011529050.1:p.Leu2308Gln
XM_011530749.1:c.6923T>A XP_011529051.1:p.Leu2308Gln
XM_011530750.1:c.6923T>A XP_011529052.1:p.Leu2308Gln
XM_011530751.1:c.6923T>A XP_011529053.1:p.Leu2308Gln
XM_011530752.1:c.6920T>A XP_011529054.1:p.Leu2307Gln
XM_011530753.1:c.6923T>A XP_011529055.1:p.Leu2308Gln
XM_011530754.1:c.6923T>A XP_011529056.1:p.Leu2308Gln
XM_011530755.1:c.6920T>A XP_011529057.1:p.Leu2307Gln
XM_011530756.1:c.6923T>A XP_011529058.1:p.Leu2308Gln
XM_011530757.1:c.6923T>A XP_011529059.1:p.Leu2308Gln
XM_011530758.1:c.6923T>A XP_011529060.1:p.Leu2308Gln
XR_938360.1:n.7358T>A
XM_005261965.4:c.6674T>A XP_005262022.1:p.Leu2225Gln
XM_011530751.2:c.6923T>A XP_011529053.1:p.Leu2308Gln
XM_017029191.1:c.7055T>A XP_016884680.1:p.Leu2352Gln
XM_017029192.1:c.7052T>A XP_016884681.1:p.Leu2351Gln
XM_017029193.1:c.7034T>A XP_016884682.1:p.Leu2345Gln
XM_017029194.1:c.7055T>A XP_016884683.1:p.Leu2352Gln
XM_017029195.1:c.7055T>A XP_016884684.1:p.Leu2352Gln
XM_017029196.1:c.7052T>A XP_016884685.1:p.Leu2351Gln
XM_017029197.1:c.7055T>A XP_016884686.1:p.Leu2352Gln
XM_017029198.2:c.6944T>A XP_016884687.1:p.Leu2315Gln
XM_017029199.1:c.6944T>A XP_016884688.1:p.Leu2315Gln
XM_017029200.1:c.6944T>A XP_016884689.1:p.Leu2315Gln
XM_017029201.1:c.6944T>A XP_016884690.1:p.Leu2315Gln
XM_017029202.1:c.6944T>A XP_016884691.1:p.Leu2315Gln
XM_017029203.1:c.6944T>A XP_016884692.1:p.Leu2315Gln
XM_017029204.1:c.6806T>A XP_016884693.1:p.Leu2269Gln
XM_017029206.1:c.7055T>A XP_016884695.1:p.Leu2352Gln
XM_024452322.1:c.6923T>A XP_024308090.1:p.Leu2308Gln
NM_031407.7:c.6674T>A MANE Select NP_113584.3:p.Leu2225Gln