Canonical Allele Identifier: CA413145428

Gene: HUWE1

Linked Data

• MyVariant Identifiers: chrX:g.53561145C>T (hg19) ; chrX:g.53534184C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53534184C>T , CM000685.2:g.53534184C>T	GRCh38
NC_000023.10:g.53561145C>T , CM000685.1:g.53561145C>T	GRCh37
NC_000023.9:g.53577870C>T	NCBI36
NG_016261.2:g.157550G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704099.1:c.12629G>A	ENSP00000515693.1:p.Trp4210Ter
ENST00000262854.11:c.12845G>A MANE Select	ENSP00000262854.6:p.Trp4282Ter
ENST00000262854.10:c.12845G>A	ENSP00000262854.6:p.Trp4282Ter
ENST00000342160.7:c.12845G>A	ENSP00000340648.3:p.Trp4282Ter
ENST00000426907.5:c.3312G>A
ENST00000488459.1:n.158G>A
ENST00000612484.4:c.12818G>A	ENSP00000479451.1:p.Trp4273Ter
NM_031407.6:c.12845G>A	NP_113584.3:p.Trp4282Ter
XM_005261965.2:c.12845G>A	XP_005262022.1:p.Trp4282Ter
XM_011530746.1:c.13094G>A	XP_011529048.1:p.Trp4365Ter
XM_011530747.1:c.13094G>A	XP_011529049.1:p.Trp4365Ter
XM_011530748.1:c.13094G>A	XP_011529050.1:p.Trp4365Ter
XM_011530749.1:c.13094G>A	XP_011529051.1:p.Trp4365Ter
XM_011530750.1:c.13094G>A	XP_011529052.1:p.Trp4365Ter
XM_011530751.1:c.13094G>A	XP_011529053.1:p.Trp4365Ter
XM_011530752.1:c.13091G>A	XP_011529054.1:p.Trp4364Ter
XM_011530753.1:c.13049G>A	XP_011529055.1:p.Trp4350Ter
XM_011530754.1:c.13046G>A	XP_011529056.1:p.Trp4349Ter
XM_011530755.1:c.13043G>A	XP_011529057.1:p.Trp4348Ter
XM_011530756.1:c.12995G>A	XP_011529058.1:p.Trp4332Ter
XM_011530757.1:c.12692G>A	XP_011529059.1:p.Trp4231Ter
XM_005261965.4:c.12845G>A	XP_005262022.1:p.Trp4282Ter
XM_011530751.2:c.13094G>A	XP_011529053.1:p.Trp4365Ter
XM_017029191.1:c.13226G>A	XP_016884680.1:p.Trp4409Ter
XM_017029192.1:c.13223G>A	XP_016884681.1:p.Trp4408Ter
XM_017029193.1:c.13205G>A	XP_016884682.1:p.Trp4402Ter
XM_017029194.1:c.13181G>A	XP_016884683.1:p.Trp4394Ter
XM_017029195.1:c.13178G>A	XP_016884684.1:p.Trp4393Ter
XM_017029196.1:c.13175G>A	XP_016884685.1:p.Trp4392Ter
XM_017029197.1:c.13127G>A	XP_016884686.1:p.Trp4376Ter
XM_017029198.2:c.13115G>A	XP_016884687.1:p.Trp4372Ter
XM_017029199.1:c.13115G>A	XP_016884688.1:p.Trp4372Ter
XM_017029200.1:c.13115G>A	XP_016884689.1:p.Trp4372Ter
XM_017029201.1:c.13115G>A	XP_016884690.1:p.Trp4372Ter
XM_017029202.1:c.13115G>A	XP_016884691.1:p.Trp4372Ter
XM_017029203.1:c.13115G>A	XP_016884692.1:p.Trp4372Ter
XM_017029204.1:c.12977G>A	XP_016884693.1:p.Trp4326Ter
XM_017029206.1:c.12824G>A	XP_016884695.1:p.Trp4275Ter
XM_024452322.1:c.13094G>A	XP_024308090.1:p.Trp4365Ter
NM_031407.7:c.12845G>A MANE Select	NP_113584.3:p.Trp4282Ter