Canonical Allele Identifier: CA413145002

Gene: HUWE1

Linked Data

• MyVariant Identifiers: chrX:g.53561113G>T (hg19) ; chrX:g.53534152G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53534152G>T , CM000685.2:g.53534152G>T	GRCh38
NC_000023.10:g.53561113G>T , CM000685.1:g.53561113G>T	GRCh37
NC_000023.9:g.53577838G>T	NCBI36
NG_016261.2:g.157582C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704099.1:c.12661C>A	ENSP00000515693.1:p.Arg4221Ser
ENST00000262854.11:c.12877C>A MANE Select	ENSP00000262854.6:p.Arg4293Ser
ENST00000262854.10:c.12877C>A	ENSP00000262854.6:p.Arg4293Ser
ENST00000342160.7:c.12877C>A	ENSP00000340648.3:p.Arg4293Ser
ENST00000426907.5:c.3344C>A
ENST00000488459.1:n.190C>A
ENST00000612484.4:c.12850C>A	ENSP00000479451.1:p.Arg4284Ser
NM_031407.6:c.12877C>A	NP_113584.3:p.Arg4293Ser
XM_005261965.2:c.12877C>A	XP_005262022.1:p.Arg4293Ser
XM_011530746.1:c.13126C>A	XP_011529048.1:p.Arg4376Ser
XM_011530747.1:c.13126C>A	XP_011529049.1:p.Arg4376Ser
XM_011530748.1:c.13126C>A	XP_011529050.1:p.Arg4376Ser
XM_011530749.1:c.13126C>A	XP_011529051.1:p.Arg4376Ser
XM_011530750.1:c.13126C>A	XP_011529052.1:p.Arg4376Ser
XM_011530751.1:c.13126C>A	XP_011529053.1:p.Arg4376Ser
XM_011530752.1:c.13123C>A	XP_011529054.1:p.Arg4375Ser
XM_011530753.1:c.13081C>A	XP_011529055.1:p.Arg4361Ser
XM_011530754.1:c.13078C>A	XP_011529056.1:p.Arg4360Ser
XM_011530755.1:c.13075C>A	XP_011529057.1:p.Arg4359Ser
XM_011530756.1:c.13027C>A	XP_011529058.1:p.Arg4343Ser
XM_011530757.1:c.12724C>A	XP_011529059.1:p.Arg4242Ser
XM_005261965.4:c.12877C>A	XP_005262022.1:p.Arg4293Ser
XM_011530751.2:c.13126C>A	XP_011529053.1:p.Arg4376Ser
XM_017029191.1:c.13258C>A	XP_016884680.1:p.Arg4420Ser
XM_017029192.1:c.13255C>A	XP_016884681.1:p.Arg4419Ser
XM_017029193.1:c.13237C>A	XP_016884682.1:p.Arg4413Ser
XM_017029194.1:c.13213C>A	XP_016884683.1:p.Arg4405Ser
XM_017029195.1:c.13210C>A	XP_016884684.1:p.Arg4404Ser
XM_017029196.1:c.13207C>A	XP_016884685.1:p.Arg4403Ser
XM_017029197.1:c.13159C>A	XP_016884686.1:p.Arg4387Ser
XM_017029198.2:c.13147C>A	XP_016884687.1:p.Arg4383Ser
XM_017029199.1:c.13147C>A	XP_016884688.1:p.Arg4383Ser
XM_017029200.1:c.13147C>A	XP_016884689.1:p.Arg4383Ser
XM_017029201.1:c.13147C>A	XP_016884690.1:p.Arg4383Ser
XM_017029202.1:c.13147C>A	XP_016884691.1:p.Arg4383Ser
XM_017029203.1:c.13147C>A	XP_016884692.1:p.Arg4383Ser
XM_017029204.1:c.13009C>A	XP_016884693.1:p.Arg4337Ser
XM_017029206.1:c.12856C>A	XP_016884695.1:p.Arg4286Ser
XM_024452322.1:c.13126C>A	XP_024308090.1:p.Arg4376Ser
NM_031407.7:c.12877C>A MANE Select	NP_113584.3:p.Arg4293Ser