Canonical Allele Identifier: CA413145456

Gene: HUWE1

Linked Data

• MyVariant Identifiers: chrX:g.53561148A>C (hg19) ; chrX:g.53534187A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53534187A>C , CM000685.2:g.53534187A>C	GRCh38
NC_000023.10:g.53561148A>C , CM000685.1:g.53561148A>C	GRCh37
NC_000023.9:g.53577873A>C	NCBI36
NG_016261.2:g.157547T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704099.1:c.12626T>G	ENSP00000515693.1:p.Phe4209Cys
ENST00000262854.11:c.12842T>G MANE Select	ENSP00000262854.6:p.Phe4281Cys
ENST00000262854.10:c.12842T>G	ENSP00000262854.6:p.Phe4281Cys
ENST00000342160.7:c.12842T>G	ENSP00000340648.3:p.Phe4281Cys
ENST00000426907.5:c.3309T>G
ENST00000488459.1:n.155T>G
ENST00000612484.4:c.12815T>G	ENSP00000479451.1:p.Phe4272Cys
NM_031407.6:c.12842T>G	NP_113584.3:p.Phe4281Cys
XM_005261965.2:c.12842T>G	XP_005262022.1:p.Phe4281Cys
XM_011530746.1:c.13091T>G	XP_011529048.1:p.Phe4364Cys
XM_011530747.1:c.13091T>G	XP_011529049.1:p.Phe4364Cys
XM_011530748.1:c.13091T>G	XP_011529050.1:p.Phe4364Cys
XM_011530749.1:c.13091T>G	XP_011529051.1:p.Phe4364Cys
XM_011530750.1:c.13091T>G	XP_011529052.1:p.Phe4364Cys
XM_011530751.1:c.13091T>G	XP_011529053.1:p.Phe4364Cys
XM_011530752.1:c.13088T>G	XP_011529054.1:p.Phe4363Cys
XM_011530753.1:c.13046T>G	XP_011529055.1:p.Phe4349Cys
XM_011530754.1:c.13043T>G	XP_011529056.1:p.Phe4348Cys
XM_011530755.1:c.13040T>G	XP_011529057.1:p.Phe4347Cys
XM_011530756.1:c.12992T>G	XP_011529058.1:p.Phe4331Cys
XM_011530757.1:c.12689T>G	XP_011529059.1:p.Phe4230Cys
XM_005261965.4:c.12842T>G	XP_005262022.1:p.Phe4281Cys
XM_011530751.2:c.13091T>G	XP_011529053.1:p.Phe4364Cys
XM_017029191.1:c.13223T>G	XP_016884680.1:p.Phe4408Cys
XM_017029192.1:c.13220T>G	XP_016884681.1:p.Phe4407Cys
XM_017029193.1:c.13202T>G	XP_016884682.1:p.Phe4401Cys
XM_017029194.1:c.13178T>G	XP_016884683.1:p.Phe4393Cys
XM_017029195.1:c.13175T>G	XP_016884684.1:p.Phe4392Cys
XM_017029196.1:c.13172T>G	XP_016884685.1:p.Phe4391Cys
XM_017029197.1:c.13124T>G	XP_016884686.1:p.Phe4375Cys
XM_017029198.2:c.13112T>G	XP_016884687.1:p.Phe4371Cys
XM_017029199.1:c.13112T>G	XP_016884688.1:p.Phe4371Cys
XM_017029200.1:c.13112T>G	XP_016884689.1:p.Phe4371Cys
XM_017029201.1:c.13112T>G	XP_016884690.1:p.Phe4371Cys
XM_017029202.1:c.13112T>G	XP_016884691.1:p.Phe4371Cys
XM_017029203.1:c.13112T>G	XP_016884692.1:p.Phe4371Cys
XM_017029204.1:c.12974T>G	XP_016884693.1:p.Phe4325Cys
XM_017029206.1:c.12821T>G	XP_016884695.1:p.Phe4274Cys
XM_024452322.1:c.13091T>G	XP_024308090.1:p.Phe4364Cys
NM_031407.7:c.12842T>G MANE Select	NP_113584.3:p.Phe4281Cys