Canonical Allele Identifier: CA2429868945
Gene: HUWE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.53534219_53534220delinsGC , CM000685.2:g.53534219_53534220delinsGC GRCh38
NC_000023.10:g.53561180_53561181delinsGC , CM000685.1:g.53561180_53561181delinsGC GRCh37
NC_000023.9:g.53577905_53577906delinsGC NCBI36
NG_016261.2:g.157514_157515delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000704099.1:c.12616-23_12616-22delinsGC ENSP00000515693.1:n.12616-23_12616-22delinsGC
ENST00000262854.11:c.12832-23_12832-22delinsGC MANE Select ENSP00000262854.6:n.12832-23_12832-22delinsGC
ENST00000262854.10:c.12832-23_12832-22delinsGC ENSP00000262854.6:n.12832-23_12832-22delinsGC
ENST00000342160.7:c.12832-23_12832-22delinsGC ENSP00000340648.3:n.12832-23_12832-22delinsGC
ENST00000426907.5:c.3299-23_3299-22delinsGC
ENST00000488459.1:n.145-23_145-22delinsGC
ENST00000612484.4:c.12805-23_12805-22delinsGC ENSP00000479451.1:n.12805-23_12805-22delinsGC
NM_031407.6:c.12832-23_12832-22delinsGC NP_113584.3:n.12832-23_12832-22delinsGC
XM_005261965.2:c.12832-23_12832-22delinsGC XP_005262022.1:n.12832-23_12832-22delinsGC
XM_011530746.1:c.13081-23_13081-22delinsGC XP_011529048.1:n.13081-23_13081-22delinsGC
XM_011530747.1:c.13081-23_13081-22delinsGC XP_011529049.1:n.13081-23_13081-22delinsGC
XM_011530748.1:c.13081-23_13081-22delinsGC XP_011529050.1:n.13081-23_13081-22delinsGC
XM_011530749.1:c.13081-23_13081-22delinsGC XP_011529051.1:n.13081-23_13081-22delinsGC
XM_011530750.1:c.13081-23_13081-22delinsGC XP_011529052.1:n.13081-23_13081-22delinsGC
XM_011530751.1:c.13081-23_13081-22delinsGC XP_011529053.1:n.13081-23_13081-22delinsGC
XM_011530752.1:c.13078-23_13078-22delinsGC XP_011529054.1:n.13078-23_13078-22delinsGC
XM_011530753.1:c.13036-23_13036-22delinsGC XP_011529055.1:n.13036-23_13036-22delinsGC
XM_011530754.1:c.13033-23_13033-22delinsGC XP_011529056.1:n.13033-23_13033-22delinsGC
XM_011530755.1:c.13030-23_13030-22delinsGC XP_011529057.1:n.13030-23_13030-22delinsGC
XM_011530756.1:c.12982-23_12982-22delinsGC XP_011529058.1:n.12982-23_12982-22delinsGC
XM_011530757.1:c.12679-23_12679-22delinsGC XP_011529059.1:n.12679-23_12679-22delinsGC
XM_005261965.4:c.12832-23_12832-22delinsGC XP_005262022.1:n.12832-23_12832-22delinsGC
XM_011530751.2:c.13081-23_13081-22delinsGC XP_011529053.1:n.13081-23_13081-22delinsGC
XM_017029191.1:c.13213-23_13213-22delinsGC XP_016884680.1:n.13213-23_13213-22delinsGC
XM_017029192.1:c.13210-23_13210-22delinsGC XP_016884681.1:n.13210-23_13210-22delinsGC
XM_017029193.1:c.13192-23_13192-22delinsGC XP_016884682.1:n.13192-23_13192-22delinsGC
XM_017029194.1:c.13168-23_13168-22delinsGC XP_016884683.1:n.13168-23_13168-22delinsGC
XM_017029195.1:c.13165-23_13165-22delinsGC XP_016884684.1:n.13165-23_13165-22delinsGC
XM_017029196.1:c.13162-23_13162-22delinsGC XP_016884685.1:n.13162-23_13162-22delinsGC
XM_017029197.1:c.13114-23_13114-22delinsGC XP_016884686.1:n.13114-23_13114-22delinsGC
XM_017029198.2:c.13102-23_13102-22delinsGC XP_016884687.1:n.13102-23_13102-22delinsGC
XM_017029199.1:c.13102-23_13102-22delinsGC XP_016884688.1:n.13102-23_13102-22delinsGC
XM_017029200.1:c.13102-23_13102-22delinsGC XP_016884689.1:n.13102-23_13102-22delinsGC
XM_017029201.1:c.13102-23_13102-22delinsGC XP_016884690.1:n.13102-23_13102-22delinsGC
XM_017029202.1:c.13102-23_13102-22delinsGC XP_016884691.1:n.13102-23_13102-22delinsGC
XM_017029203.1:c.13102-23_13102-22delinsGC XP_016884692.1:n.13102-23_13102-22delinsGC
XM_017029204.1:c.12964-23_12964-22delinsGC XP_016884693.1:n.12964-23_12964-22delinsGC
XM_017029206.1:c.12811-23_12811-22delinsGC XP_016884695.1:n.12811-23_12811-22delinsGC
XM_024452322.1:c.13081-23_13081-22delinsGC XP_024308090.1:n.13081-23_13081-22delinsGC
NM_031407.7:c.12832-23_12832-22delinsGC MANE Select NP_113584.3:n.12832-23_12832-22delinsGC