Canonical Allele Identifier: CA516419315

Gene: HUWE1

Linked Data

• MyVariant Identifiers: chrX:g.53561114G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53534153G>A , CM000685.2:g.53534153G>A	GRCh38
NC_000023.10:g.53561114G>A , CM000685.1:g.53561114G>A	GRCh37
NC_000023.9:g.53577839G>A	NCBI36
NG_016261.2:g.157581C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704099.1:c.12660C>T	ENSP00000515693.1:p.Asp4220=
ENST00000262854.11:c.12876C>T MANE Select	ENSP00000262854.6:p.Asp4292=
ENST00000262854.10:c.12876C>T	ENSP00000262854.6:p.Asp4292=
ENST00000342160.7:c.12876C>T	ENSP00000340648.3:p.Asp4292=
ENST00000426907.5:c.3343C>T
ENST00000488459.1:n.189C>T
ENST00000612484.4:c.12849C>T	ENSP00000479451.1:p.Asp4283=
NM_031407.6:c.12876C>T	NP_113584.3:p.Asp4292=
XM_005261965.2:c.12876C>T	XP_005262022.1:p.Asp4292=
XM_011530746.1:c.13125C>T	XP_011529048.1:p.Asp4375=
XM_011530747.1:c.13125C>T	XP_011529049.1:p.Asp4375=
XM_011530748.1:c.13125C>T	XP_011529050.1:p.Asp4375=
XM_011530749.1:c.13125C>T	XP_011529051.1:p.Asp4375=
XM_011530750.1:c.13125C>T	XP_011529052.1:p.Asp4375=
XM_011530751.1:c.13125C>T	XP_011529053.1:p.Asp4375=
XM_011530752.1:c.13122C>T	XP_011529054.1:p.Asp4374=
XM_011530753.1:c.13080C>T	XP_011529055.1:p.Asp4360=
XM_011530754.1:c.13077C>T	XP_011529056.1:p.Asp4359=
XM_011530755.1:c.13074C>T	XP_011529057.1:p.Asp4358=
XM_011530756.1:c.13026C>T	XP_011529058.1:p.Asp4342=
XM_011530757.1:c.12723C>T	XP_011529059.1:p.Asp4241=
XM_005261965.4:c.12876C>T	XP_005262022.1:p.Asp4292=
XM_011530751.2:c.13125C>T	XP_011529053.1:p.Asp4375=
XM_017029191.1:c.13257C>T	XP_016884680.1:p.Asp4419=
XM_017029192.1:c.13254C>T	XP_016884681.1:p.Asp4418=
XM_017029193.1:c.13236C>T	XP_016884682.1:p.Asp4412=
XM_017029194.1:c.13212C>T	XP_016884683.1:p.Asp4404=
XM_017029195.1:c.13209C>T	XP_016884684.1:p.Asp4403=
XM_017029196.1:c.13206C>T	XP_016884685.1:p.Asp4402=
XM_017029197.1:c.13158C>T	XP_016884686.1:p.Asp4386=
XM_017029198.2:c.13146C>T	XP_016884687.1:p.Asp4382=
XM_017029199.1:c.13146C>T	XP_016884688.1:p.Asp4382=
XM_017029200.1:c.13146C>T	XP_016884689.1:p.Asp4382=
XM_017029201.1:c.13146C>T	XP_016884690.1:p.Asp4382=
XM_017029202.1:c.13146C>T	XP_016884691.1:p.Asp4382=
XM_017029203.1:c.13146C>T	XP_016884692.1:p.Asp4382=
XM_017029204.1:c.13008C>T	XP_016884693.1:p.Asp4336=
XM_017029206.1:c.12855C>T	XP_016884695.1:p.Asp4285=
XM_024452322.1:c.13125C>T	XP_024308090.1:p.Asp4375=
NM_031407.7:c.12876C>T MANE Select	NP_113584.3:p.Asp4292=