Canonical Allele Identifier: CA516418938

Gene: HUWE1

Linked Data

• MyVariant Identifiers: chrX:g.53561075C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53534114C>T , CM000685.2:g.53534114C>T	GRCh38
NC_000023.10:g.53561075C>T , CM000685.1:g.53561075C>T	GRCh37
NC_000023.9:g.53577800C>T	NCBI36
NG_016261.2:g.157620G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704099.1:c.12699G>A	ENSP00000515693.1:p.Lys4233=
ENST00000262854.11:c.12915G>A MANE Select	ENSP00000262854.6:p.Lys4305=
ENST00000262854.10:c.12915G>A	ENSP00000262854.6:p.Lys4305=
ENST00000342160.7:c.12915G>A	ENSP00000340648.3:p.Lys4305=
ENST00000426907.5:c.3382G>A
ENST00000488459.1:n.228G>A
ENST00000612484.4:c.12888G>A	ENSP00000479451.1:p.Lys4296=
NM_031407.6:c.12915G>A	NP_113584.3:p.Lys4305=
XM_005261965.2:c.12915G>A	XP_005262022.1:p.Lys4305=
XM_011530746.1:c.13164G>A	XP_011529048.1:p.Lys4388=
XM_011530747.1:c.13164G>A	XP_011529049.1:p.Lys4388=
XM_011530748.1:c.13164G>A	XP_011529050.1:p.Lys4388=
XM_011530749.1:c.13164G>A	XP_011529051.1:p.Lys4388=
XM_011530750.1:c.13164G>A	XP_011529052.1:p.Lys4388=
XM_011530751.1:c.13164G>A	XP_011529053.1:p.Lys4388=
XM_011530752.1:c.13161G>A	XP_011529054.1:p.Lys4387=
XM_011530753.1:c.13119G>A	XP_011529055.1:p.Lys4373=
XM_011530754.1:c.13116G>A	XP_011529056.1:p.Lys4372=
XM_011530755.1:c.13113G>A	XP_011529057.1:p.Lys4371=
XM_011530756.1:c.13065G>A	XP_011529058.1:p.Lys4355=
XM_011530757.1:c.12762G>A	XP_011529059.1:p.Lys4254=
XM_005261965.4:c.12915G>A	XP_005262022.1:p.Lys4305=
XM_011530751.2:c.13164G>A	XP_011529053.1:p.Lys4388=
XM_017029191.1:c.13296G>A	XP_016884680.1:p.Lys4432=
XM_017029192.1:c.13293G>A	XP_016884681.1:p.Lys4431=
XM_017029193.1:c.13275G>A	XP_016884682.1:p.Lys4425=
XM_017029194.1:c.13251G>A	XP_016884683.1:p.Lys4417=
XM_017029195.1:c.13248G>A	XP_016884684.1:p.Lys4416=
XM_017029196.1:c.13245G>A	XP_016884685.1:p.Lys4415=
XM_017029197.1:c.13197G>A	XP_016884686.1:p.Lys4399=
XM_017029198.2:c.13185G>A	XP_016884687.1:p.Lys4395=
XM_017029199.1:c.13185G>A	XP_016884688.1:p.Lys4395=
XM_017029200.1:c.13185G>A	XP_016884689.1:p.Lys4395=
XM_017029201.1:c.13185G>A	XP_016884690.1:p.Lys4395=
XM_017029202.1:c.13185G>A	XP_016884691.1:p.Lys4395=
XM_017029203.1:c.13185G>A	XP_016884692.1:p.Lys4395=
XM_017029204.1:c.13047G>A	XP_016884693.1:p.Lys4349=
XM_017029206.1:c.12894G>A	XP_016884695.1:p.Lys4298=
XM_024452322.1:c.13164G>A	XP_024308090.1:p.Lys4388=
NM_031407.7:c.12915G>A MANE Select	NP_113584.3:p.Lys4305=