Canonical Allele Identifier: CA516418241

Gene: HUWE1

Linked Data

• MyVariant Identifiers: chrX:g.53560985C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53534024C>A , CM000685.2:g.53534024C>A	GRCh38
NC_000023.10:g.53560985C>A , CM000685.1:g.53560985C>A	GRCh37
NC_000023.9:g.53577710C>A	NCBI36
NG_016261.2:g.157710G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704099.1:c.12789G>T	ENSP00000515693.1:p.Leu4263=
ENST00000262854.11:c.13005G>T MANE Select	ENSP00000262854.6:p.Leu4335=
ENST00000262854.10:c.13005G>T	ENSP00000262854.6:p.Leu4335=
ENST00000342160.7:c.13005G>T	ENSP00000340648.3:p.Leu4335=
ENST00000426907.5:c.3472G>T
ENST00000488459.1:n.318G>T
ENST00000612484.4:c.12978G>T	ENSP00000479451.1:p.Leu4326=
NM_031407.6:c.13005G>T	NP_113584.3:p.Leu4335=
XM_005261965.2:c.13005G>T	XP_005262022.1:p.Leu4335=
XM_011530746.1:c.13254G>T	XP_011529048.1:p.Leu4418=
XM_011530747.1:c.13254G>T	XP_011529049.1:p.Leu4418=
XM_011530748.1:c.13254G>T	XP_011529050.1:p.Leu4418=
XM_011530749.1:c.13254G>T	XP_011529051.1:p.Leu4418=
XM_011530750.1:c.13254G>T	XP_011529052.1:p.Leu4418=
XM_011530751.1:c.13254G>T	XP_011529053.1:p.Leu4418=
XM_011530752.1:c.13251G>T	XP_011529054.1:p.Leu4417=
XM_011530753.1:c.13209G>T	XP_011529055.1:p.Leu4403=
XM_011530754.1:c.13206G>T	XP_011529056.1:p.Leu4402=
XM_011530755.1:c.13203G>T	XP_011529057.1:p.Leu4401=
XM_011530756.1:c.13155G>T	XP_011529058.1:p.Leu4385=
XM_011530757.1:c.12852G>T	XP_011529059.1:p.Leu4284=
XM_005261965.4:c.13005G>T	XP_005262022.1:p.Leu4335=
XM_011530751.2:c.13254G>T	XP_011529053.1:p.Leu4418=
XM_017029191.1:c.13386G>T	XP_016884680.1:p.Leu4462=
XM_017029192.1:c.13383G>T	XP_016884681.1:p.Leu4461=
XM_017029193.1:c.13365G>T	XP_016884682.1:p.Leu4455=
XM_017029194.1:c.13341G>T	XP_016884683.1:p.Leu4447=
XM_017029195.1:c.13338G>T	XP_016884684.1:p.Leu4446=
XM_017029196.1:c.13335G>T	XP_016884685.1:p.Leu4445=
XM_017029197.1:c.13287G>T	XP_016884686.1:p.Leu4429=
XM_017029198.2:c.13275G>T	XP_016884687.1:p.Leu4425=
XM_017029199.1:c.13275G>T	XP_016884688.1:p.Leu4425=
XM_017029200.1:c.13275G>T	XP_016884689.1:p.Leu4425=
XM_017029201.1:c.13275G>T	XP_016884690.1:p.Leu4425=
XM_017029202.1:c.13275G>T	XP_016884691.1:p.Leu4425=
XM_017029203.1:c.13275G>T	XP_016884692.1:p.Leu4425=
XM_017029204.1:c.13137G>T	XP_016884693.1:p.Leu4379=
XM_017029206.1:c.12984G>T	XP_016884695.1:p.Leu4328=
XM_024452322.1:c.13254G>T	XP_024308090.1:p.Leu4418=
NM_031407.7:c.13005G>T MANE Select	NP_113584.3:p.Leu4335=