Canonical Allele Identifier: CA413143776

Gene: HUWE1

Linked Data

• MyVariant Identifiers: chrX:g.53561006A>C (hg19) ; chrX:g.53534045A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53534045A>C , CM000685.2:g.53534045A>C	GRCh38
NC_000023.10:g.53561006A>C , CM000685.1:g.53561006A>C	GRCh37
NC_000023.9:g.53577731A>C	NCBI36
NG_016261.2:g.157689T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704099.1:c.12768T>G	ENSP00000515693.1:p.Asp4256Glu
ENST00000262854.11:c.12984T>G MANE Select	ENSP00000262854.6:p.Asp4328Glu
ENST00000262854.10:c.12984T>G	ENSP00000262854.6:p.Asp4328Glu
ENST00000342160.7:c.12984T>G	ENSP00000340648.3:p.Asp4328Glu
ENST00000426907.5:c.3451T>G
ENST00000488459.1:n.297T>G
ENST00000612484.4:c.12957T>G	ENSP00000479451.1:p.Asp4319Glu
NM_031407.6:c.12984T>G	NP_113584.3:p.Asp4328Glu
XM_005261965.2:c.12984T>G	XP_005262022.1:p.Asp4328Glu
XM_011530746.1:c.13233T>G	XP_011529048.1:p.Asp4411Glu
XM_011530747.1:c.13233T>G	XP_011529049.1:p.Asp4411Glu
XM_011530748.1:c.13233T>G	XP_011529050.1:p.Asp4411Glu
XM_011530749.1:c.13233T>G	XP_011529051.1:p.Asp4411Glu
XM_011530750.1:c.13233T>G	XP_011529052.1:p.Asp4411Glu
XM_011530751.1:c.13233T>G	XP_011529053.1:p.Asp4411Glu
XM_011530752.1:c.13230T>G	XP_011529054.1:p.Asp4410Glu
XM_011530753.1:c.13188T>G	XP_011529055.1:p.Asp4396Glu
XM_011530754.1:c.13185T>G	XP_011529056.1:p.Asp4395Glu
XM_011530755.1:c.13182T>G	XP_011529057.1:p.Asp4394Glu
XM_011530756.1:c.13134T>G	XP_011529058.1:p.Asp4378Glu
XM_011530757.1:c.12831T>G	XP_011529059.1:p.Asp4277Glu
XM_005261965.4:c.12984T>G	XP_005262022.1:p.Asp4328Glu
XM_011530751.2:c.13233T>G	XP_011529053.1:p.Asp4411Glu
XM_017029191.1:c.13365T>G	XP_016884680.1:p.Asp4455Glu
XM_017029192.1:c.13362T>G	XP_016884681.1:p.Asp4454Glu
XM_017029193.1:c.13344T>G	XP_016884682.1:p.Asp4448Glu
XM_017029194.1:c.13320T>G	XP_016884683.1:p.Asp4440Glu
XM_017029195.1:c.13317T>G	XP_016884684.1:p.Asp4439Glu
XM_017029196.1:c.13314T>G	XP_016884685.1:p.Asp4438Glu
XM_017029197.1:c.13266T>G	XP_016884686.1:p.Asp4422Glu
XM_017029198.2:c.13254T>G	XP_016884687.1:p.Asp4418Glu
XM_017029199.1:c.13254T>G	XP_016884688.1:p.Asp4418Glu
XM_017029200.1:c.13254T>G	XP_016884689.1:p.Asp4418Glu
XM_017029201.1:c.13254T>G	XP_016884690.1:p.Asp4418Glu
XM_017029202.1:c.13254T>G	XP_016884691.1:p.Asp4418Glu
XM_017029203.1:c.13254T>G	XP_016884692.1:p.Asp4418Glu
XM_017029204.1:c.13116T>G	XP_016884693.1:p.Asp4372Glu
XM_017029206.1:c.12963T>G	XP_016884695.1:p.Asp4321Glu
XM_024452322.1:c.13233T>G	XP_024308090.1:p.Asp4411Glu
NM_031407.7:c.12984T>G MANE Select	NP_113584.3:p.Asp4328Glu