Canonical Allele Identifier: CA413143467

Gene: HUWE1

Linked Data

• MyVariant Identifiers: chrX:g.53560968C>T (hg19) ; chrX:g.53534007C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53534007C>T , CM000685.2:g.53534007C>T	GRCh38
NC_000023.10:g.53560968C>T , CM000685.1:g.53560968C>T	GRCh37
NC_000023.9:g.53577693C>T	NCBI36
NG_016261.2:g.157727G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704099.1:c.12806G>A	ENSP00000515693.1:p.Cys4269Tyr
ENST00000262854.11:c.13022G>A MANE Select	ENSP00000262854.6:p.Cys4341Tyr
ENST00000262854.10:c.13022G>A	ENSP00000262854.6:p.Cys4341Tyr
ENST00000342160.7:c.13022G>A	ENSP00000340648.3:p.Cys4341Tyr
ENST00000426907.5:c.3489G>A
ENST00000488459.1:n.335G>A
ENST00000612484.4:c.12995G>A	ENSP00000479451.1:p.Cys4332Tyr
NM_031407.6:c.13022G>A	NP_113584.3:p.Cys4341Tyr
XM_005261965.2:c.13022G>A	XP_005262022.1:p.Cys4341Tyr
XM_011530746.1:c.13271G>A	XP_011529048.1:p.Cys4424Tyr
XM_011530747.1:c.13271G>A	XP_011529049.1:p.Cys4424Tyr
XM_011530748.1:c.13271G>A	XP_011529050.1:p.Cys4424Tyr
XM_011530749.1:c.13271G>A	XP_011529051.1:p.Cys4424Tyr
XM_011530750.1:c.13271G>A	XP_011529052.1:p.Cys4424Tyr
XM_011530751.1:c.13271G>A	XP_011529053.1:p.Cys4424Tyr
XM_011530752.1:c.13268G>A	XP_011529054.1:p.Cys4423Tyr
XM_011530753.1:c.13226G>A	XP_011529055.1:p.Cys4409Tyr
XM_011530754.1:c.13223G>A	XP_011529056.1:p.Cys4408Tyr
XM_011530755.1:c.13220G>A	XP_011529057.1:p.Cys4407Tyr
XM_011530756.1:c.13172G>A	XP_011529058.1:p.Cys4391Tyr
XM_011530757.1:c.12869G>A	XP_011529059.1:p.Cys4290Tyr
XM_005261965.4:c.13022G>A	XP_005262022.1:p.Cys4341Tyr
XM_011530751.2:c.13271G>A	XP_011529053.1:p.Cys4424Tyr
XM_017029191.1:c.13403G>A	XP_016884680.1:p.Cys4468Tyr
XM_017029192.1:c.13400G>A	XP_016884681.1:p.Cys4467Tyr
XM_017029193.1:c.13382G>A	XP_016884682.1:p.Cys4461Tyr
XM_017029194.1:c.13358G>A	XP_016884683.1:p.Cys4453Tyr
XM_017029195.1:c.13355G>A	XP_016884684.1:p.Cys4452Tyr
XM_017029196.1:c.13352G>A	XP_016884685.1:p.Cys4451Tyr
XM_017029197.1:c.13304G>A	XP_016884686.1:p.Cys4435Tyr
XM_017029198.2:c.13292G>A	XP_016884687.1:p.Cys4431Tyr
XM_017029199.1:c.13292G>A	XP_016884688.1:p.Cys4431Tyr
XM_017029200.1:c.13292G>A	XP_016884689.1:p.Cys4431Tyr
XM_017029201.1:c.13292G>A	XP_016884690.1:p.Cys4431Tyr
XM_017029202.1:c.13292G>A	XP_016884691.1:p.Cys4431Tyr
XM_017029203.1:c.13292G>A	XP_016884692.1:p.Cys4431Tyr
XM_017029204.1:c.13154G>A	XP_016884693.1:p.Cys4385Tyr
XM_017029206.1:c.13001G>A	XP_016884695.1:p.Cys4334Tyr
XM_024452322.1:c.13271G>A	XP_024308090.1:p.Cys4424Tyr
NM_031407.7:c.13022G>A MANE Select	NP_113584.3:p.Cys4341Tyr