Canonical Allele Identifier: CA516420342

Gene: HUWE1

Linked Data

• MyVariant Identifiers: chrX:g.53561513G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53534552G>A , CM000685.2:g.53534552G>A	GRCh38
NC_000023.10:g.53561513G>A , CM000685.1:g.53561513G>A	GRCh37
NC_000023.9:g.53578238G>A	NCBI36
NG_016261.2:g.157182C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704099.1:c.12579C>T	ENSP00000515693.1:p.Asn4193=
ENST00000262854.11:c.12795C>T MANE Select	ENSP00000262854.6:p.Asn4265=
ENST00000262854.10:c.12795C>T	ENSP00000262854.6:p.Asn4265=
ENST00000342160.7:c.12795C>T	ENSP00000340648.3:p.Asn4265=
ENST00000426907.5:c.3262C>T
ENST00000488459.1:n.108C>T
ENST00000612484.4:c.12768C>T	ENSP00000479451.1:p.Asn4256=
NM_031407.6:c.12795C>T	NP_113584.3:p.Asn4265=
XM_005261965.2:c.12795C>T	XP_005262022.1:p.Asn4265=
XM_011530746.1:c.13044C>T	XP_011529048.1:p.Asn4348=
XM_011530747.1:c.13044C>T	XP_011529049.1:p.Asn4348=
XM_011530748.1:c.13044C>T	XP_011529050.1:p.Asn4348=
XM_011530749.1:c.13044C>T	XP_011529051.1:p.Asn4348=
XM_011530750.1:c.13044C>T	XP_011529052.1:p.Asn4348=
XM_011530751.1:c.13044C>T	XP_011529053.1:p.Asn4348=
XM_011530752.1:c.13041C>T	XP_011529054.1:p.Asn4347=
XM_011530753.1:c.12999C>T	XP_011529055.1:p.Asn4333=
XM_011530754.1:c.12996C>T	XP_011529056.1:p.Asn4332=
XM_011530755.1:c.12993C>T	XP_011529057.1:p.Asn4331=
XM_011530756.1:c.12945C>T	XP_011529058.1:p.Asn4315=
XM_011530757.1:c.12642C>T	XP_011529059.1:p.Asn4214=
XM_005261965.4:c.12795C>T	XP_005262022.1:p.Asn4265=
XM_011530751.2:c.13044C>T	XP_011529053.1:p.Asn4348=
XM_017029191.1:c.13176C>T	XP_016884680.1:p.Asn4392=
XM_017029192.1:c.13173C>T	XP_016884681.1:p.Asn4391=
XM_017029193.1:c.13155C>T	XP_016884682.1:p.Asn4385=
XM_017029194.1:c.13131C>T	XP_016884683.1:p.Asn4377=
XM_017029195.1:c.13128C>T	XP_016884684.1:p.Asn4376=
XM_017029196.1:c.13125C>T	XP_016884685.1:p.Asn4375=
XM_017029197.1:c.13077C>T	XP_016884686.1:p.Asn4359=
XM_017029198.2:c.13065C>T	XP_016884687.1:p.Asn4355=
XM_017029199.1:c.13065C>T	XP_016884688.1:p.Asn4355=
XM_017029200.1:c.13065C>T	XP_016884689.1:p.Asn4355=
XM_017029201.1:c.13065C>T	XP_016884690.1:p.Asn4355=
XM_017029202.1:c.13065C>T	XP_016884691.1:p.Asn4355=
XM_017029203.1:c.13065C>T	XP_016884692.1:p.Asn4355=
XM_017029204.1:c.12927C>T	XP_016884693.1:p.Asn4309=
XM_017029206.1:c.12774C>T	XP_016884695.1:p.Asn4258=
XM_024452322.1:c.13044C>T	XP_024308090.1:p.Asn4348=
NM_031407.7:c.12795C>T MANE Select	NP_113584.3:p.Asn4265=