Canonical Allele Identifier: CA2579616548
Gene: HUWE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.53534721_53534722del , CM000685.2:g.53534721_53534722del GRCh38
NC_000023.10:g.53561682_53561683del , CM000685.1:g.53561682_53561683del GRCh37
NC_000023.9:g.53578407_53578408del NCBI36
NG_016261.2:g.157013_157014del

Transcript Alleles

HGVS Amino-acid Change
ENST00000704099.1:c.12434-24_12434-23del ENSP00000515693.1:n.12434-24_12434-23del
ENST00000262854.11:c.12650-24_12650-23del MANE Select ENSP00000262854.6:n.12650-24_12650-23del
ENST00000262854.10:c.12650-24_12650-23del ENSP00000262854.6:n.12650-24_12650-23del
ENST00000342160.7:c.12650-24_12650-23del ENSP00000340648.3:n.12650-24_12650-23del
ENST00000426907.5:c.3117-24_3117-23del
ENST00000612484.4:c.12623-24_12623-23del ENSP00000479451.1:n.12623-24_12623-23del
NM_031407.6:c.12650-24_12650-23del NP_113584.3:n.12650-24_12650-23del
XM_005261965.2:c.12650-24_12650-23del XP_005262022.1:n.12650-24_12650-23del
XM_011530746.1:c.12899-24_12899-23del XP_011529048.1:n.12899-24_12899-23del
XM_011530747.1:c.12899-24_12899-23del XP_011529049.1:n.12899-24_12899-23del
XM_011530748.1:c.12899-24_12899-23del XP_011529050.1:n.12899-24_12899-23del
XM_011530749.1:c.12899-24_12899-23del XP_011529051.1:n.12899-24_12899-23del
XM_011530750.1:c.12899-24_12899-23del XP_011529052.1:n.12899-24_12899-23del
XM_011530751.1:c.12899-24_12899-23del XP_011529053.1:n.12899-24_12899-23del
XM_011530752.1:c.12896-24_12896-23del XP_011529054.1:n.12896-24_12896-23del
XM_011530753.1:c.12854-24_12854-23del XP_011529055.1:n.12854-24_12854-23del
XM_011530754.1:c.12851-24_12851-23del XP_011529056.1:n.12851-24_12851-23del
XM_011530755.1:c.12848-24_12848-23del XP_011529057.1:n.12848-24_12848-23del
XM_011530756.1:c.12800-24_12800-23del XP_011529058.1:n.12800-24_12800-23del
XM_011530757.1:c.12497-24_12497-23del XP_011529059.1:n.12497-24_12497-23del
XM_005261965.4:c.12650-24_12650-23del XP_005262022.1:n.12650-24_12650-23del
XM_011530751.2:c.12899-24_12899-23del XP_011529053.1:n.12899-24_12899-23del
XM_017029191.1:c.13031-24_13031-23del XP_016884680.1:n.13031-24_13031-23del
XM_017029192.1:c.13028-24_13028-23del XP_016884681.1:n.13028-24_13028-23del
XM_017029193.1:c.13010-24_13010-23del XP_016884682.1:n.13010-24_13010-23del
XM_017029194.1:c.12986-24_12986-23del XP_016884683.1:n.12986-24_12986-23del
XM_017029195.1:c.12983-24_12983-23del XP_016884684.1:n.12983-24_12983-23del
XM_017029196.1:c.12980-24_12980-23del XP_016884685.1:n.12980-24_12980-23del
XM_017029197.1:c.12932-24_12932-23del XP_016884686.1:n.12932-24_12932-23del
XM_017029198.2:c.12920-24_12920-23del XP_016884687.1:n.12920-24_12920-23del
XM_017029199.1:c.12920-24_12920-23del XP_016884688.1:n.12920-24_12920-23del
XM_017029200.1:c.12920-24_12920-23del XP_016884689.1:n.12920-24_12920-23del
XM_017029201.1:c.12920-24_12920-23del XP_016884690.1:n.12920-24_12920-23del
XM_017029202.1:c.12920-24_12920-23del XP_016884691.1:n.12920-24_12920-23del
XM_017029203.1:c.12920-24_12920-23del XP_016884692.1:n.12920-24_12920-23del
XM_017029204.1:c.12782-24_12782-23del XP_016884693.1:n.12782-24_12782-23del
XM_017029206.1:c.12629-24_12629-23del XP_016884695.1:n.12629-24_12629-23del
XM_024452322.1:c.12899-24_12899-23del XP_024308090.1:n.12899-24_12899-23del
NM_031407.7:c.12650-24_12650-23del MANE Select NP_113584.3:n.12650-24_12650-23del