Canonical Allele Identifier: CA2693810098

Gene: HUWE1

Linked Data

• gnomAD v4: X-53533720-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53533723del , CM000685.2:g.53533723del	GRCh38
NC_000023.10:g.53560684del , CM000685.1:g.53560684del	GRCh37
NC_000023.9:g.53577409del	NCBI36
NG_016261.2:g.158013del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704099.1:c.12806+286del	ENSP00000515693.1:n.12806+286del
ENST00000262854.11:c.13022+286del MANE Select	ENSP00000262854.6:n.13022+286del
ENST00000262854.10:c.13022+286del	ENSP00000262854.6:n.13022+286del
ENST00000342160.7:c.13022+286del	ENSP00000340648.3:n.13022+286del
ENST00000426907.5:c.3489+286del
ENST00000488459.1:n.621del
ENST00000612484.4:c.12995+286del	ENSP00000479451.1:n.12995+286del
NM_031407.6:c.13022+286del	NP_113584.3:n.13022+286del
XM_005261965.2:c.13022+286del	XP_005262022.1:n.13022+286del
XM_011530746.1:c.13271+286del	XP_011529048.1:n.13271+286del
XM_011530747.1:c.13271+286del	XP_011529049.1:n.13271+286del
XM_011530748.1:c.13271+286del	XP_011529050.1:n.13271+286del
XM_011530749.1:c.13271+286del	XP_011529051.1:n.13271+286del
XM_011530750.1:c.13271+286del	XP_011529052.1:n.13271+286del
XM_011530751.1:c.13271+286del	XP_011529053.1:n.13271+286del
XM_011530752.1:c.13268+286del	XP_011529054.1:n.13268+286del
XM_011530753.1:c.13226+286del	XP_011529055.1:n.13226+286del
XM_011530754.1:c.13223+286del	XP_011529056.1:n.13223+286del
XM_011530755.1:c.13220+286del	XP_011529057.1:n.13220+286del
XM_011530756.1:c.13172+286del	XP_011529058.1:n.13172+286del
XM_011530757.1:c.12869+286del	XP_011529059.1:n.12869+286del
XM_005261965.4:c.13022+286del	XP_005262022.1:n.13022+286del
XM_011530751.2:c.13271+286del	XP_011529053.1:n.13271+286del
XM_017029191.1:c.13403+286del	XP_016884680.1:n.13403+286del
XM_017029192.1:c.13400+286del	XP_016884681.1:n.13400+286del
XM_017029193.1:c.13382+286del	XP_016884682.1:n.13382+286del
XM_017029194.1:c.13358+286del	XP_016884683.1:n.13358+286del
XM_017029195.1:c.13355+286del	XP_016884684.1:n.13355+286del
XM_017029196.1:c.13352+286del	XP_016884685.1:n.13352+286del
XM_017029197.1:c.13304+286del	XP_016884686.1:n.13304+286del
XM_017029198.2:c.13292+286del	XP_016884687.1:n.13292+286del
XM_017029199.1:c.13292+286del	XP_016884688.1:n.13292+286del
XM_017029200.1:c.13292+286del	XP_016884689.1:n.13292+286del
XM_017029201.1:c.13292+286del	XP_016884690.1:n.13292+286del
XM_017029202.1:c.13292+286del	XP_016884691.1:n.13292+286del
XM_017029203.1:c.13292+286del	XP_016884692.1:n.13292+286del
XM_017029204.1:c.13154+286del	XP_016884693.1:n.13154+286del
XM_017029206.1:c.13001+286del	XP_016884695.1:n.13001+286del
XM_024452322.1:c.13271+286del	XP_024308090.1:n.13271+286del
NM_031407.7:c.13022+286del MANE Select	NP_113584.3:n.13022+286del