Canonical Allele Identifier: CA516423721

Gene: HUWE1

Linked Data

• MyVariant Identifiers: chrX:g.53564561A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53537600A>G , CM000685.2:g.53537600A>G	GRCh38
NC_000023.10:g.53564561A>G , CM000685.1:g.53564561A>G	GRCh37
NC_000023.9:g.53581286A>G	NCBI36
NG_016261.2:g.154134T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704099.1:c.11877T>C	ENSP00000515693.1:p.Tyr3959=
ENST00000262854.11:c.12093T>C MANE Select	ENSP00000262854.6:p.Tyr4031=
ENST00000262854.10:c.12093T>C	ENSP00000262854.6:p.Tyr4031=
ENST00000342160.7:c.12093T>C	ENSP00000340648.3:p.Tyr4031=
ENST00000426907.5:c.2560T>C
ENST00000480438.1:n.228T>C
ENST00000612484.4:c.12066T>C	ENSP00000479451.1:p.Tyr4022=
NM_031407.6:c.12093T>C	NP_113584.3:p.Tyr4031=
XM_005261965.2:c.12093T>C	XP_005262022.1:p.Tyr4031=
XM_011530746.1:c.12342T>C	XP_011529048.1:p.Tyr4114=
XM_011530747.1:c.12342T>C	XP_011529049.1:p.Tyr4114=
XM_011530748.1:c.12342T>C	XP_011529050.1:p.Tyr4114=
XM_011530749.1:c.12342T>C	XP_011529051.1:p.Tyr4114=
XM_011530750.1:c.12342T>C	XP_011529052.1:p.Tyr4114=
XM_011530751.1:c.12342T>C	XP_011529053.1:p.Tyr4114=
XM_011530752.1:c.12339T>C	XP_011529054.1:p.Tyr4113=
XM_011530753.1:c.12297T>C	XP_011529055.1:p.Tyr4099=
XM_011530754.1:c.12294T>C	XP_011529056.1:p.Tyr4098=
XM_011530755.1:c.12291T>C	XP_011529057.1:p.Tyr4097=
XM_011530756.1:c.12243T>C	XP_011529058.1:p.Tyr4081=
XM_011530757.1:c.11940T>C	XP_011529059.1:p.Tyr3980=
XM_005261965.4:c.12093T>C	XP_005262022.1:p.Tyr4031=
XM_011530751.2:c.12342T>C	XP_011529053.1:p.Tyr4114=
XM_017029191.1:c.12474T>C	XP_016884680.1:p.Tyr4158=
XM_017029192.1:c.12471T>C	XP_016884681.1:p.Tyr4157=
XM_017029193.1:c.12453T>C	XP_016884682.1:p.Tyr4151=
XM_017029194.1:c.12429T>C	XP_016884683.1:p.Tyr4143=
XM_017029195.1:c.12426T>C	XP_016884684.1:p.Tyr4142=
XM_017029196.1:c.12423T>C	XP_016884685.1:p.Tyr4141=
XM_017029197.1:c.12375T>C	XP_016884686.1:p.Tyr4125=
XM_017029198.2:c.12363T>C	XP_016884687.1:p.Tyr4121=
XM_017029199.1:c.12363T>C	XP_016884688.1:p.Tyr4121=
XM_017029200.1:c.12363T>C	XP_016884689.1:p.Tyr4121=
XM_017029201.1:c.12363T>C	XP_016884690.1:p.Tyr4121=
XM_017029202.1:c.12363T>C	XP_016884691.1:p.Tyr4121=
XM_017029203.1:c.12363T>C	XP_016884692.1:p.Tyr4121=
XM_017029204.1:c.12225T>C	XP_016884693.1:p.Tyr4075=
XM_017029206.1:c.12072T>C	XP_016884695.1:p.Tyr4024=
XM_024452322.1:c.12342T>C	XP_024308090.1:p.Tyr4114=
NM_031407.7:c.12093T>C MANE Select	NP_113584.3:p.Tyr4031=