Canonical Allele Identifier: CA2429869018
Gene: HUWE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.53534364_53534365delinsTA , CM000685.2:g.53534364_53534365delinsTA GRCh38
NC_000023.10:g.53561325_53561326delinsTA , CM000685.1:g.53561325_53561326delinsTA GRCh37
NC_000023.9:g.53578050_53578051delinsTA NCBI36
NG_016261.2:g.157369_157370delinsTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000704099.1:c.12615+151_12615+152delinsTA ENSP00000515693.1:n.12615+151_12615+152delinsTA
ENST00000262854.11:c.12831+151_12831+152delinsTA MANE Select ENSP00000262854.6:n.12831+151_12831+152delinsTA
ENST00000262854.10:c.12831+151_12831+152delinsTA ENSP00000262854.6:n.12831+151_12831+152delinsTA
ENST00000342160.7:c.12831+151_12831+152delinsTA ENSP00000340648.3:n.12831+151_12831+152delinsTA
ENST00000426907.5:c.3298+151_3298+152delinsTA
ENST00000488459.1:n.144+151_144+152delinsTA
ENST00000612484.4:c.12804+151_12804+152delinsTA ENSP00000479451.1:n.12804+151_12804+152delinsTA
NM_031407.6:c.12831+151_12831+152delinsTA NP_113584.3:n.12831+151_12831+152delinsTA
XM_005261965.2:c.12831+151_12831+152delinsTA XP_005262022.1:n.12831+151_12831+152delinsTA
XM_011530746.1:c.13080+151_13080+152delinsTA XP_011529048.1:n.13080+151_13080+152delinsTA
XM_011530747.1:c.13080+151_13080+152delinsTA XP_011529049.1:n.13080+151_13080+152delinsTA
XM_011530748.1:c.13080+151_13080+152delinsTA XP_011529050.1:n.13080+151_13080+152delinsTA
XM_011530749.1:c.13080+151_13080+152delinsTA XP_011529051.1:n.13080+151_13080+152delinsTA
XM_011530750.1:c.13080+151_13080+152delinsTA XP_011529052.1:n.13080+151_13080+152delinsTA
XM_011530751.1:c.13080+151_13080+152delinsTA XP_011529053.1:n.13080+151_13080+152delinsTA
XM_011530752.1:c.13077+151_13077+152delinsTA XP_011529054.1:n.13077+151_13077+152delinsTA
XM_011530753.1:c.13035+151_13035+152delinsTA XP_011529055.1:n.13035+151_13035+152delinsTA
XM_011530754.1:c.13032+151_13032+152delinsTA XP_011529056.1:n.13032+151_13032+152delinsTA
XM_011530755.1:c.13029+151_13029+152delinsTA XP_011529057.1:n.13029+151_13029+152delinsTA
XM_011530756.1:c.12981+151_12981+152delinsTA XP_011529058.1:n.12981+151_12981+152delinsTA
XM_011530757.1:c.12678+151_12678+152delinsTA XP_011529059.1:n.12678+151_12678+152delinsTA
XM_005261965.4:c.12831+151_12831+152delinsTA XP_005262022.1:n.12831+151_12831+152delinsTA
XM_011530751.2:c.13080+151_13080+152delinsTA XP_011529053.1:n.13080+151_13080+152delinsTA
XM_017029191.1:c.13212+151_13212+152delinsTA XP_016884680.1:n.13212+151_13212+152delinsTA
XM_017029192.1:c.13209+151_13209+152delinsTA XP_016884681.1:n.13209+151_13209+152delinsTA
XM_017029193.1:c.13191+151_13191+152delinsTA XP_016884682.1:n.13191+151_13191+152delinsTA
XM_017029194.1:c.13167+151_13167+152delinsTA XP_016884683.1:n.13167+151_13167+152delinsTA
XM_017029195.1:c.13164+151_13164+152delinsTA XP_016884684.1:n.13164+151_13164+152delinsTA
XM_017029196.1:c.13161+151_13161+152delinsTA XP_016884685.1:n.13161+151_13161+152delinsTA
XM_017029197.1:c.13113+151_13113+152delinsTA XP_016884686.1:n.13113+151_13113+152delinsTA
XM_017029198.2:c.13101+151_13101+152delinsTA XP_016884687.1:n.13101+151_13101+152delinsTA
XM_017029199.1:c.13101+151_13101+152delinsTA XP_016884688.1:n.13101+151_13101+152delinsTA
XM_017029200.1:c.13101+151_13101+152delinsTA XP_016884689.1:n.13101+151_13101+152delinsTA
XM_017029201.1:c.13101+151_13101+152delinsTA XP_016884690.1:n.13101+151_13101+152delinsTA
XM_017029202.1:c.13101+151_13101+152delinsTA XP_016884691.1:n.13101+151_13101+152delinsTA
XM_017029203.1:c.13101+151_13101+152delinsTA XP_016884692.1:n.13101+151_13101+152delinsTA
XM_017029204.1:c.12963+151_12963+152delinsTA XP_016884693.1:n.12963+151_12963+152delinsTA
XM_017029206.1:c.12810+151_12810+152delinsTA XP_016884695.1:n.12810+151_12810+152delinsTA
XM_024452322.1:c.13080+151_13080+152delinsTA XP_024308090.1:n.13080+151_13080+152delinsTA
NM_031407.7:c.12831+151_12831+152delinsTA MANE Select NP_113584.3:n.12831+151_12831+152delinsTA