Canonical Allele Identifier: CA2693810326
Gene: HUWE1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.53534330_53534331insATCCCA , CM000685.2:g.53534330_53534331insATCCCA GRCh38
NC_000023.10:g.53561291_53561292insATCCCA , CM000685.1:g.53561291_53561292insATCCCA GRCh37
NC_000023.9:g.53578016_53578017insATCCCA NCBI36
NG_016261.2:g.157403_157404insTGGGAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000704099.1:c.12616-134_12616-133insTGGGAT ENSP00000515693.1:n.12616-134_12616-133insTGGGAT
ENST00000262854.11:c.12832-134_12832-133insTGGGAT MANE Select ENSP00000262854.6:n.12832-134_12832-133insTGGGAT
ENST00000262854.10:c.12832-134_12832-133insTGGGAT ENSP00000262854.6:n.12832-134_12832-133insTGGGAT
ENST00000342160.7:c.12832-134_12832-133insTGGGAT ENSP00000340648.3:n.12832-134_12832-133insTGGGAT
ENST00000426907.5:c.3299-134_3299-133insTGGGAT
ENST00000488459.1:n.145-134_145-133insTGGGAT
ENST00000612484.4:c.12805-134_12805-133insTGGGAT ENSP00000479451.1:n.12805-134_12805-133insTGGGAT
NM_031407.6:c.12832-134_12832-133insTGGGAT NP_113584.3:n.12832-134_12832-133insTGGGAT
XM_005261965.2:c.12832-134_12832-133insTGGGAT XP_005262022.1:n.12832-134_12832-133insTGGGAT
XM_011530746.1:c.13081-134_13081-133insTGGGAT XP_011529048.1:n.13081-134_13081-133insTGGGAT
XM_011530747.1:c.13081-134_13081-133insTGGGAT XP_011529049.1:n.13081-134_13081-133insTGGGAT
XM_011530748.1:c.13081-134_13081-133insTGGGAT XP_011529050.1:n.13081-134_13081-133insTGGGAT
XM_011530749.1:c.13081-134_13081-133insTGGGAT XP_011529051.1:n.13081-134_13081-133insTGGGAT
XM_011530750.1:c.13081-134_13081-133insTGGGAT XP_011529052.1:n.13081-134_13081-133insTGGGAT
XM_011530751.1:c.13081-134_13081-133insTGGGAT XP_011529053.1:n.13081-134_13081-133insTGGGAT
XM_011530752.1:c.13078-134_13078-133insTGGGAT XP_011529054.1:n.13078-134_13078-133insTGGGAT
XM_011530753.1:c.13036-134_13036-133insTGGGAT XP_011529055.1:n.13036-134_13036-133insTGGGAT
XM_011530754.1:c.13033-134_13033-133insTGGGAT XP_011529056.1:n.13033-134_13033-133insTGGGAT
XM_011530755.1:c.13030-134_13030-133insTGGGAT XP_011529057.1:n.13030-134_13030-133insTGGGAT
XM_011530756.1:c.12982-134_12982-133insTGGGAT XP_011529058.1:n.12982-134_12982-133insTGGGAT
XM_011530757.1:c.12679-134_12679-133insTGGGAT XP_011529059.1:n.12679-134_12679-133insTGGGAT
XM_005261965.4:c.12832-134_12832-133insTGGGAT XP_005262022.1:n.12832-134_12832-133insTGGGAT
XM_011530751.2:c.13081-134_13081-133insTGGGAT XP_011529053.1:n.13081-134_13081-133insTGGGAT
XM_017029191.1:c.13213-134_13213-133insTGGGAT XP_016884680.1:n.13213-134_13213-133insTGGGAT
XM_017029192.1:c.13210-134_13210-133insTGGGAT XP_016884681.1:n.13210-134_13210-133insTGGGAT
XM_017029193.1:c.13192-134_13192-133insTGGGAT XP_016884682.1:n.13192-134_13192-133insTGGGAT
XM_017029194.1:c.13168-134_13168-133insTGGGAT XP_016884683.1:n.13168-134_13168-133insTGGGAT
XM_017029195.1:c.13165-134_13165-133insTGGGAT XP_016884684.1:n.13165-134_13165-133insTGGGAT
XM_017029196.1:c.13162-134_13162-133insTGGGAT XP_016884685.1:n.13162-134_13162-133insTGGGAT
XM_017029197.1:c.13114-134_13114-133insTGGGAT XP_016884686.1:n.13114-134_13114-133insTGGGAT
XM_017029198.2:c.13102-134_13102-133insTGGGAT XP_016884687.1:n.13102-134_13102-133insTGGGAT
XM_017029199.1:c.13102-134_13102-133insTGGGAT XP_016884688.1:n.13102-134_13102-133insTGGGAT
XM_017029200.1:c.13102-134_13102-133insTGGGAT XP_016884689.1:n.13102-134_13102-133insTGGGAT
XM_017029201.1:c.13102-134_13102-133insTGGGAT XP_016884690.1:n.13102-134_13102-133insTGGGAT
XM_017029202.1:c.13102-134_13102-133insTGGGAT XP_016884691.1:n.13102-134_13102-133insTGGGAT
XM_017029203.1:c.13102-134_13102-133insTGGGAT XP_016884692.1:n.13102-134_13102-133insTGGGAT
XM_017029204.1:c.12964-134_12964-133insTGGGAT XP_016884693.1:n.12964-134_12964-133insTGGGAT
XM_017029206.1:c.12811-134_12811-133insTGGGAT XP_016884695.1:n.12811-134_12811-133insTGGGAT
XM_024452322.1:c.13081-134_13081-133insTGGGAT XP_024308090.1:n.13081-134_13081-133insTGGGAT
NM_031407.7:c.12832-134_12832-133insTGGGAT MANE Select NP_113584.3:n.12832-134_12832-133insTGGGAT