Canonical Allele Identifier: CA413146059

Gene: HUWE1

Linked Data

• MyVariant Identifiers: chrX:g.53561515T>C (hg19) ; chrX:g.53534554T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53534554T>C , CM000685.2:g.53534554T>C	GRCh38
NC_000023.10:g.53561515T>C , CM000685.1:g.53561515T>C	GRCh37
NC_000023.9:g.53578240T>C	NCBI36
NG_016261.2:g.157180A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704099.1:c.12577A>G	ENSP00000515693.1:p.Asn4193Asp
ENST00000262854.11:c.12793A>G MANE Select	ENSP00000262854.6:p.Asn4265Asp
ENST00000262854.10:c.12793A>G	ENSP00000262854.6:p.Asn4265Asp
ENST00000342160.7:c.12793A>G	ENSP00000340648.3:p.Asn4265Asp
ENST00000426907.5:c.3260A>G
ENST00000488459.1:n.106A>G
ENST00000612484.4:c.12766A>G	ENSP00000479451.1:p.Asn4256Asp
NM_031407.6:c.12793A>G	NP_113584.3:p.Asn4265Asp
XM_005261965.2:c.12793A>G	XP_005262022.1:p.Asn4265Asp
XM_011530746.1:c.13042A>G	XP_011529048.1:p.Asn4348Asp
XM_011530747.1:c.13042A>G	XP_011529049.1:p.Asn4348Asp
XM_011530748.1:c.13042A>G	XP_011529050.1:p.Asn4348Asp
XM_011530749.1:c.13042A>G	XP_011529051.1:p.Asn4348Asp
XM_011530750.1:c.13042A>G	XP_011529052.1:p.Asn4348Asp
XM_011530751.1:c.13042A>G	XP_011529053.1:p.Asn4348Asp
XM_011530752.1:c.13039A>G	XP_011529054.1:p.Asn4347Asp
XM_011530753.1:c.12997A>G	XP_011529055.1:p.Asn4333Asp
XM_011530754.1:c.12994A>G	XP_011529056.1:p.Asn4332Asp
XM_011530755.1:c.12991A>G	XP_011529057.1:p.Asn4331Asp
XM_011530756.1:c.12943A>G	XP_011529058.1:p.Asn4315Asp
XM_011530757.1:c.12640A>G	XP_011529059.1:p.Asn4214Asp
XM_005261965.4:c.12793A>G	XP_005262022.1:p.Asn4265Asp
XM_011530751.2:c.13042A>G	XP_011529053.1:p.Asn4348Asp
XM_017029191.1:c.13174A>G	XP_016884680.1:p.Asn4392Asp
XM_017029192.1:c.13171A>G	XP_016884681.1:p.Asn4391Asp
XM_017029193.1:c.13153A>G	XP_016884682.1:p.Asn4385Asp
XM_017029194.1:c.13129A>G	XP_016884683.1:p.Asn4377Asp
XM_017029195.1:c.13126A>G	XP_016884684.1:p.Asn4376Asp
XM_017029196.1:c.13123A>G	XP_016884685.1:p.Asn4375Asp
XM_017029197.1:c.13075A>G	XP_016884686.1:p.Asn4359Asp
XM_017029198.2:c.13063A>G	XP_016884687.1:p.Asn4355Asp
XM_017029199.1:c.13063A>G	XP_016884688.1:p.Asn4355Asp
XM_017029200.1:c.13063A>G	XP_016884689.1:p.Asn4355Asp
XM_017029201.1:c.13063A>G	XP_016884690.1:p.Asn4355Asp
XM_017029202.1:c.13063A>G	XP_016884691.1:p.Asn4355Asp
XM_017029203.1:c.13063A>G	XP_016884692.1:p.Asn4355Asp
XM_017029204.1:c.12925A>G	XP_016884693.1:p.Asn4309Asp
XM_017029206.1:c.12772A>G	XP_016884695.1:p.Asn4258Asp
XM_024452322.1:c.13042A>G	XP_024308090.1:p.Asn4348Asp
NM_031407.7:c.12793A>G MANE Select	NP_113584.3:p.Asn4265Asp