Canonical Allele Identifier: CA2429868820
Gene: HUWE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.53533863T= , CM000685.2:g.53533863T= GRCh38
NC_000023.10:g.53560824T= , CM000685.1:g.53560824T= GRCh37
NC_000023.9:g.53577549T= NCBI36
NG_016261.2:g.157871A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000704099.1:c.12806+144A= ENSP00000515693.1:n.12806+144A=
ENST00000262854.11:c.13022+144A= MANE Select ENSP00000262854.6:n.13022+144A=
ENST00000262854.10:c.13022+144A= ENSP00000262854.6:n.13022+144A=
ENST00000342160.7:c.13022+144A= ENSP00000340648.3:n.13022+144A=
ENST00000426907.5:c.3489+144A=
ENST00000488459.1:n.479A=
ENST00000612484.4:c.12995+144A= ENSP00000479451.1:n.12995+144A=
NM_031407.6:c.13022+144A= NP_113584.3:n.13022+144A=
XM_005261965.2:c.13022+144A= XP_005262022.1:n.13022+144A=
XM_011530746.1:c.13271+144A= XP_011529048.1:n.13271+144A=
XM_011530747.1:c.13271+144A= XP_011529049.1:n.13271+144A=
XM_011530748.1:c.13271+144A= XP_011529050.1:n.13271+144A=
XM_011530749.1:c.13271+144A= XP_011529051.1:n.13271+144A=
XM_011530750.1:c.13271+144A= XP_011529052.1:n.13271+144A=
XM_011530751.1:c.13271+144A= XP_011529053.1:n.13271+144A=
XM_011530752.1:c.13268+144A= XP_011529054.1:n.13268+144A=
XM_011530753.1:c.13226+144A= XP_011529055.1:n.13226+144A=
XM_011530754.1:c.13223+144A= XP_011529056.1:n.13223+144A=
XM_011530755.1:c.13220+144A= XP_011529057.1:n.13220+144A=
XM_011530756.1:c.13172+144A= XP_011529058.1:n.13172+144A=
XM_011530757.1:c.12869+144A= XP_011529059.1:n.12869+144A=
XM_005261965.4:c.13022+144A= XP_005262022.1:n.13022+144A=
XM_011530751.2:c.13271+144A= XP_011529053.1:n.13271+144A=
XM_017029191.1:c.13403+144A= XP_016884680.1:n.13403+144A=
XM_017029192.1:c.13400+144A= XP_016884681.1:n.13400+144A=
XM_017029193.1:c.13382+144A= XP_016884682.1:n.13382+144A=
XM_017029194.1:c.13358+144A= XP_016884683.1:n.13358+144A=
XM_017029195.1:c.13355+144A= XP_016884684.1:n.13355+144A=
XM_017029196.1:c.13352+144A= XP_016884685.1:n.13352+144A=
XM_017029197.1:c.13304+144A= XP_016884686.1:n.13304+144A=
XM_017029198.2:c.13292+144A= XP_016884687.1:n.13292+144A=
XM_017029199.1:c.13292+144A= XP_016884688.1:n.13292+144A=
XM_017029200.1:c.13292+144A= XP_016884689.1:n.13292+144A=
XM_017029201.1:c.13292+144A= XP_016884690.1:n.13292+144A=
XM_017029202.1:c.13292+144A= XP_016884691.1:n.13292+144A=
XM_017029203.1:c.13292+144A= XP_016884692.1:n.13292+144A=
XM_017029204.1:c.13154+144A= XP_016884693.1:n.13154+144A=
XM_017029206.1:c.13001+144A= XP_016884695.1:n.13001+144A=
XM_024452322.1:c.13271+144A= XP_024308090.1:n.13271+144A=
NM_031407.7:c.13022+144A= MANE Select NP_113584.3:n.13022+144A=