Canonical Allele Identifier: CA413145180

Gene: HUWE1

Linked Data

• gnomAD v4: X-53534164-C-A
• MyVariant Identifiers: chrX:g.53561125C>A (hg19) ; chrX:g.53534164C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53534164C>A , CM000685.2:g.53534164C>A	GRCh38
NC_000023.10:g.53561125C>A , CM000685.1:g.53561125C>A	GRCh37
NC_000023.9:g.53577850C>A	NCBI36
NG_016261.2:g.157570G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704099.1:c.12649G>T	ENSP00000515693.1:p.Asp4217Tyr
ENST00000262854.11:c.12865G>T MANE Select	ENSP00000262854.6:p.Asp4289Tyr
ENST00000262854.10:c.12865G>T	ENSP00000262854.6:p.Asp4289Tyr
ENST00000342160.7:c.12865G>T	ENSP00000340648.3:p.Asp4289Tyr
ENST00000426907.5:c.3332G>T
ENST00000488459.1:n.178G>T
ENST00000612484.4:c.12838G>T	ENSP00000479451.1:p.Asp4280Tyr
NM_031407.6:c.12865G>T	NP_113584.3:p.Asp4289Tyr
XM_005261965.2:c.12865G>T	XP_005262022.1:p.Asp4289Tyr
XM_011530746.1:c.13114G>T	XP_011529048.1:p.Asp4372Tyr
XM_011530747.1:c.13114G>T	XP_011529049.1:p.Asp4372Tyr
XM_011530748.1:c.13114G>T	XP_011529050.1:p.Asp4372Tyr
XM_011530749.1:c.13114G>T	XP_011529051.1:p.Asp4372Tyr
XM_011530750.1:c.13114G>T	XP_011529052.1:p.Asp4372Tyr
XM_011530751.1:c.13114G>T	XP_011529053.1:p.Asp4372Tyr
XM_011530752.1:c.13111G>T	XP_011529054.1:p.Asp4371Tyr
XM_011530753.1:c.13069G>T	XP_011529055.1:p.Asp4357Tyr
XM_011530754.1:c.13066G>T	XP_011529056.1:p.Asp4356Tyr
XM_011530755.1:c.13063G>T	XP_011529057.1:p.Asp4355Tyr
XM_011530756.1:c.13015G>T	XP_011529058.1:p.Asp4339Tyr
XM_011530757.1:c.12712G>T	XP_011529059.1:p.Asp4238Tyr
XM_005261965.4:c.12865G>T	XP_005262022.1:p.Asp4289Tyr
XM_011530751.2:c.13114G>T	XP_011529053.1:p.Asp4372Tyr
XM_017029191.1:c.13246G>T	XP_016884680.1:p.Asp4416Tyr
XM_017029192.1:c.13243G>T	XP_016884681.1:p.Asp4415Tyr
XM_017029193.1:c.13225G>T	XP_016884682.1:p.Asp4409Tyr
XM_017029194.1:c.13201G>T	XP_016884683.1:p.Asp4401Tyr
XM_017029195.1:c.13198G>T	XP_016884684.1:p.Asp4400Tyr
XM_017029196.1:c.13195G>T	XP_016884685.1:p.Asp4399Tyr
XM_017029197.1:c.13147G>T	XP_016884686.1:p.Asp4383Tyr
XM_017029198.2:c.13135G>T	XP_016884687.1:p.Asp4379Tyr
XM_017029199.1:c.13135G>T	XP_016884688.1:p.Asp4379Tyr
XM_017029200.1:c.13135G>T	XP_016884689.1:p.Asp4379Tyr
XM_017029201.1:c.13135G>T	XP_016884690.1:p.Asp4379Tyr
XM_017029202.1:c.13135G>T	XP_016884691.1:p.Asp4379Tyr
XM_017029203.1:c.13135G>T	XP_016884692.1:p.Asp4379Tyr
XM_017029204.1:c.12997G>T	XP_016884693.1:p.Asp4333Tyr
XM_017029206.1:c.12844G>T	XP_016884695.1:p.Asp4282Tyr
XM_024452322.1:c.13114G>T	XP_024308090.1:p.Asp4372Tyr
NM_031407.7:c.12865G>T MANE Select	NP_113584.3:p.Asp4289Tyr