Canonical Allele Identifier: CA413145786

Gene: HUWE1

Linked Data

• MyVariant Identifiers: chrX:g.53561482T>A (hg19) ; chrX:g.53534521T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53534521T>A , CM000685.2:g.53534521T>A	GRCh38
NC_000023.10:g.53561482T>A , CM000685.1:g.53561482T>A	GRCh37
NC_000023.9:g.53578207T>A	NCBI36
NG_016261.2:g.157213A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704099.1:c.12610A>T	ENSP00000515693.1:p.Ile4204Phe
ENST00000262854.11:c.12826A>T MANE Select	ENSP00000262854.6:p.Ile4276Phe
ENST00000262854.10:c.12826A>T	ENSP00000262854.6:p.Ile4276Phe
ENST00000342160.7:c.12826A>T	ENSP00000340648.3:p.Ile4276Phe
ENST00000426907.5:c.3293A>T
ENST00000488459.1:n.139A>T
ENST00000612484.4:c.12799A>T	ENSP00000479451.1:p.Ile4267Phe
NM_031407.6:c.12826A>T	NP_113584.3:p.Ile4276Phe
XM_005261965.2:c.12826A>T	XP_005262022.1:p.Ile4276Phe
XM_011530746.1:c.13075A>T	XP_011529048.1:p.Ile4359Phe
XM_011530747.1:c.13075A>T	XP_011529049.1:p.Ile4359Phe
XM_011530748.1:c.13075A>T	XP_011529050.1:p.Ile4359Phe
XM_011530749.1:c.13075A>T	XP_011529051.1:p.Ile4359Phe
XM_011530750.1:c.13075A>T	XP_011529052.1:p.Ile4359Phe
XM_011530751.1:c.13075A>T	XP_011529053.1:p.Ile4359Phe
XM_011530752.1:c.13072A>T	XP_011529054.1:p.Ile4358Phe
XM_011530753.1:c.13030A>T	XP_011529055.1:p.Ile4344Phe
XM_011530754.1:c.13027A>T	XP_011529056.1:p.Ile4343Phe
XM_011530755.1:c.13024A>T	XP_011529057.1:p.Ile4342Phe
XM_011530756.1:c.12976A>T	XP_011529058.1:p.Ile4326Phe
XM_011530757.1:c.12673A>T	XP_011529059.1:p.Ile4225Phe
XM_005261965.4:c.12826A>T	XP_005262022.1:p.Ile4276Phe
XM_011530751.2:c.13075A>T	XP_011529053.1:p.Ile4359Phe
XM_017029191.1:c.13207A>T	XP_016884680.1:p.Ile4403Phe
XM_017029192.1:c.13204A>T	XP_016884681.1:p.Ile4402Phe
XM_017029193.1:c.13186A>T	XP_016884682.1:p.Ile4396Phe
XM_017029194.1:c.13162A>T	XP_016884683.1:p.Ile4388Phe
XM_017029195.1:c.13159A>T	XP_016884684.1:p.Ile4387Phe
XM_017029196.1:c.13156A>T	XP_016884685.1:p.Ile4386Phe
XM_017029197.1:c.13108A>T	XP_016884686.1:p.Ile4370Phe
XM_017029198.2:c.13096A>T	XP_016884687.1:p.Ile4366Phe
XM_017029199.1:c.13096A>T	XP_016884688.1:p.Ile4366Phe
XM_017029200.1:c.13096A>T	XP_016884689.1:p.Ile4366Phe
XM_017029201.1:c.13096A>T	XP_016884690.1:p.Ile4366Phe
XM_017029202.1:c.13096A>T	XP_016884691.1:p.Ile4366Phe
XM_017029203.1:c.13096A>T	XP_016884692.1:p.Ile4366Phe
XM_017029204.1:c.12958A>T	XP_016884693.1:p.Ile4320Phe
XM_017029206.1:c.12805A>T	XP_016884695.1:p.Ile4269Phe
XM_024452322.1:c.13075A>T	XP_024308090.1:p.Ile4359Phe
NM_031407.7:c.12826A>T MANE Select	NP_113584.3:p.Ile4276Phe