Canonical Allele Identifier: CA413146174

Gene: HUWE1

Linked Data

• MyVariant Identifiers: chrX:g.53561527C>G (hg19) ; chrX:g.53534566C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53534566C>G , CM000685.2:g.53534566C>G	GRCh38
NC_000023.10:g.53561527C>G , CM000685.1:g.53561527C>G	GRCh37
NC_000023.9:g.53578252C>G	NCBI36
NG_016261.2:g.157168G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704099.1:c.12565G>C	ENSP00000515693.1:p.Asp4189His
ENST00000262854.11:c.12781G>C MANE Select	ENSP00000262854.6:p.Asp4261His
ENST00000262854.10:c.12781G>C	ENSP00000262854.6:p.Asp4261His
ENST00000342160.7:c.12781G>C	ENSP00000340648.3:p.Asp4261His
ENST00000426907.5:c.3248G>C
ENST00000488459.1:n.94G>C
ENST00000612484.4:c.12754G>C	ENSP00000479451.1:p.Asp4252His
NM_031407.6:c.12781G>C	NP_113584.3:p.Asp4261His
XM_005261965.2:c.12781G>C	XP_005262022.1:p.Asp4261His
XM_011530746.1:c.13030G>C	XP_011529048.1:p.Asp4344His
XM_011530747.1:c.13030G>C	XP_011529049.1:p.Asp4344His
XM_011530748.1:c.13030G>C	XP_011529050.1:p.Asp4344His
XM_011530749.1:c.13030G>C	XP_011529051.1:p.Asp4344His
XM_011530750.1:c.13030G>C	XP_011529052.1:p.Asp4344His
XM_011530751.1:c.13030G>C	XP_011529053.1:p.Asp4344His
XM_011530752.1:c.13027G>C	XP_011529054.1:p.Asp4343His
XM_011530753.1:c.12985G>C	XP_011529055.1:p.Asp4329His
XM_011530754.1:c.12982G>C	XP_011529056.1:p.Asp4328His
XM_011530755.1:c.12979G>C	XP_011529057.1:p.Asp4327His
XM_011530756.1:c.12931G>C	XP_011529058.1:p.Asp4311His
XM_011530757.1:c.12628G>C	XP_011529059.1:p.Asp4210His
XM_005261965.4:c.12781G>C	XP_005262022.1:p.Asp4261His
XM_011530751.2:c.13030G>C	XP_011529053.1:p.Asp4344His
XM_017029191.1:c.13162G>C	XP_016884680.1:p.Asp4388His
XM_017029192.1:c.13159G>C	XP_016884681.1:p.Asp4387His
XM_017029193.1:c.13141G>C	XP_016884682.1:p.Asp4381His
XM_017029194.1:c.13117G>C	XP_016884683.1:p.Asp4373His
XM_017029195.1:c.13114G>C	XP_016884684.1:p.Asp4372His
XM_017029196.1:c.13111G>C	XP_016884685.1:p.Asp4371His
XM_017029197.1:c.13063G>C	XP_016884686.1:p.Asp4355His
XM_017029198.2:c.13051G>C	XP_016884687.1:p.Asp4351His
XM_017029199.1:c.13051G>C	XP_016884688.1:p.Asp4351His
XM_017029200.1:c.13051G>C	XP_016884689.1:p.Asp4351His
XM_017029201.1:c.13051G>C	XP_016884690.1:p.Asp4351His
XM_017029202.1:c.13051G>C	XP_016884691.1:p.Asp4351His
XM_017029203.1:c.13051G>C	XP_016884692.1:p.Asp4351His
XM_017029204.1:c.12913G>C	XP_016884693.1:p.Asp4305His
XM_017029206.1:c.12760G>C	XP_016884695.1:p.Asp4254His
XM_024452322.1:c.13030G>C	XP_024308090.1:p.Asp4344His
NM_031407.7:c.12781G>C MANE Select	NP_113584.3:p.Asp4261His