Canonical Allele Identifier: CA413146594

Gene: HUWE1

Linked Data

• MyVariant Identifiers: chrX:g.53561578C>A (hg19) ; chrX:g.53534617C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53534617C>A , CM000685.2:g.53534617C>A	GRCh38
NC_000023.10:g.53561578C>A , CM000685.1:g.53561578C>A	GRCh37
NC_000023.9:g.53578303C>A	NCBI36
NG_016261.2:g.157117G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704099.1:c.12514G>T	ENSP00000515693.1:p.Glu4172Ter
ENST00000262854.11:c.12730G>T MANE Select	ENSP00000262854.6:p.Glu4244Ter
ENST00000262854.10:c.12730G>T	ENSP00000262854.6:p.Glu4244Ter
ENST00000342160.7:c.12730G>T	ENSP00000340648.3:p.Glu4244Ter
ENST00000426907.5:c.3197G>T
ENST00000488459.1:n.43G>T
ENST00000612484.4:c.12703G>T	ENSP00000479451.1:p.Glu4235Ter
NM_031407.6:c.12730G>T	NP_113584.3:p.Glu4244Ter
XM_005261965.2:c.12730G>T	XP_005262022.1:p.Glu4244Ter
XM_011530746.1:c.12979G>T	XP_011529048.1:p.Glu4327Ter
XM_011530747.1:c.12979G>T	XP_011529049.1:p.Glu4327Ter
XM_011530748.1:c.12979G>T	XP_011529050.1:p.Glu4327Ter
XM_011530749.1:c.12979G>T	XP_011529051.1:p.Glu4327Ter
XM_011530750.1:c.12979G>T	XP_011529052.1:p.Glu4327Ter
XM_011530751.1:c.12979G>T	XP_011529053.1:p.Glu4327Ter
XM_011530752.1:c.12976G>T	XP_011529054.1:p.Glu4326Ter
XM_011530753.1:c.12934G>T	XP_011529055.1:p.Glu4312Ter
XM_011530754.1:c.12931G>T	XP_011529056.1:p.Glu4311Ter
XM_011530755.1:c.12928G>T	XP_011529057.1:p.Glu4310Ter
XM_011530756.1:c.12880G>T	XP_011529058.1:p.Glu4294Ter
XM_011530757.1:c.12577G>T	XP_011529059.1:p.Glu4193Ter
XM_005261965.4:c.12730G>T	XP_005262022.1:p.Glu4244Ter
XM_011530751.2:c.12979G>T	XP_011529053.1:p.Glu4327Ter
XM_017029191.1:c.13111G>T	XP_016884680.1:p.Glu4371Ter
XM_017029192.1:c.13108G>T	XP_016884681.1:p.Glu4370Ter
XM_017029193.1:c.13090G>T	XP_016884682.1:p.Glu4364Ter
XM_017029194.1:c.13066G>T	XP_016884683.1:p.Glu4356Ter
XM_017029195.1:c.13063G>T	XP_016884684.1:p.Glu4355Ter
XM_017029196.1:c.13060G>T	XP_016884685.1:p.Glu4354Ter
XM_017029197.1:c.13012G>T	XP_016884686.1:p.Glu4338Ter
XM_017029198.2:c.13000G>T	XP_016884687.1:p.Glu4334Ter
XM_017029199.1:c.13000G>T	XP_016884688.1:p.Glu4334Ter
XM_017029200.1:c.13000G>T	XP_016884689.1:p.Glu4334Ter
XM_017029201.1:c.13000G>T	XP_016884690.1:p.Glu4334Ter
XM_017029202.1:c.13000G>T	XP_016884691.1:p.Glu4334Ter
XM_017029203.1:c.13000G>T	XP_016884692.1:p.Glu4334Ter
XM_017029204.1:c.12862G>T	XP_016884693.1:p.Glu4288Ter
XM_017029206.1:c.12709G>T	XP_016884695.1:p.Glu4237Ter
XM_024452322.1:c.12979G>T	XP_024308090.1:p.Glu4327Ter
NM_031407.7:c.12730G>T MANE Select	NP_113584.3:p.Glu4244Ter