Canonical Allele Identifier: CA413143553

Gene: HUWE1

Linked Data

• MyVariant Identifiers: chrX:g.53560977G>T (hg19) ; chrX:g.53534016G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53534016G>T , CM000685.2:g.53534016G>T	GRCh38
NC_000023.10:g.53560977G>T , CM000685.1:g.53560977G>T	GRCh37
NC_000023.9:g.53577702G>T	NCBI36
NG_016261.2:g.157718C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704099.1:c.12797C>A	ENSP00000515693.1:p.Ala4266Asp
ENST00000262854.11:c.13013C>A MANE Select	ENSP00000262854.6:p.Ala4338Asp
ENST00000262854.10:c.13013C>A	ENSP00000262854.6:p.Ala4338Asp
ENST00000342160.7:c.13013C>A	ENSP00000340648.3:p.Ala4338Asp
ENST00000426907.5:c.3480C>A
ENST00000488459.1:n.326C>A
ENST00000612484.4:c.12986C>A	ENSP00000479451.1:p.Ala4329Asp
NM_031407.6:c.13013C>A	NP_113584.3:p.Ala4338Asp
XM_005261965.2:c.13013C>A	XP_005262022.1:p.Ala4338Asp
XM_011530746.1:c.13262C>A	XP_011529048.1:p.Ala4421Asp
XM_011530747.1:c.13262C>A	XP_011529049.1:p.Ala4421Asp
XM_011530748.1:c.13262C>A	XP_011529050.1:p.Ala4421Asp
XM_011530749.1:c.13262C>A	XP_011529051.1:p.Ala4421Asp
XM_011530750.1:c.13262C>A	XP_011529052.1:p.Ala4421Asp
XM_011530751.1:c.13262C>A	XP_011529053.1:p.Ala4421Asp
XM_011530752.1:c.13259C>A	XP_011529054.1:p.Ala4420Asp
XM_011530753.1:c.13217C>A	XP_011529055.1:p.Ala4406Asp
XM_011530754.1:c.13214C>A	XP_011529056.1:p.Ala4405Asp
XM_011530755.1:c.13211C>A	XP_011529057.1:p.Ala4404Asp
XM_011530756.1:c.13163C>A	XP_011529058.1:p.Ala4388Asp
XM_011530757.1:c.12860C>A	XP_011529059.1:p.Ala4287Asp
XM_005261965.4:c.13013C>A	XP_005262022.1:p.Ala4338Asp
XM_011530751.2:c.13262C>A	XP_011529053.1:p.Ala4421Asp
XM_017029191.1:c.13394C>A	XP_016884680.1:p.Ala4465Asp
XM_017029192.1:c.13391C>A	XP_016884681.1:p.Ala4464Asp
XM_017029193.1:c.13373C>A	XP_016884682.1:p.Ala4458Asp
XM_017029194.1:c.13349C>A	XP_016884683.1:p.Ala4450Asp
XM_017029195.1:c.13346C>A	XP_016884684.1:p.Ala4449Asp
XM_017029196.1:c.13343C>A	XP_016884685.1:p.Ala4448Asp
XM_017029197.1:c.13295C>A	XP_016884686.1:p.Ala4432Asp
XM_017029198.2:c.13283C>A	XP_016884687.1:p.Ala4428Asp
XM_017029199.1:c.13283C>A	XP_016884688.1:p.Ala4428Asp
XM_017029200.1:c.13283C>A	XP_016884689.1:p.Ala4428Asp
XM_017029201.1:c.13283C>A	XP_016884690.1:p.Ala4428Asp
XM_017029202.1:c.13283C>A	XP_016884691.1:p.Ala4428Asp
XM_017029203.1:c.13283C>A	XP_016884692.1:p.Ala4428Asp
XM_017029204.1:c.13145C>A	XP_016884693.1:p.Ala4382Asp
XM_017029206.1:c.12992C>A	XP_016884695.1:p.Ala4331Asp
XM_024452322.1:c.13262C>A	XP_024308090.1:p.Ala4421Asp
NM_031407.7:c.13013C>A MANE Select	NP_113584.3:p.Ala4338Asp