Canonical Allele Identifier: CA413146089

Gene: HUWE1

Linked Data

• MyVariant Identifiers: chrX:g.53561517G>T (hg19) ; chrX:g.53534556G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53534556G>T , CM000685.2:g.53534556G>T	GRCh38
NC_000023.10:g.53561517G>T , CM000685.1:g.53561517G>T	GRCh37
NC_000023.9:g.53578242G>T	NCBI36
NG_016261.2:g.157178C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704099.1:c.12575C>A	ENSP00000515693.1:p.Ser4192Tyr
ENST00000262854.11:c.12791C>A MANE Select	ENSP00000262854.6:p.Ser4264Tyr
ENST00000262854.10:c.12791C>A	ENSP00000262854.6:p.Ser4264Tyr
ENST00000342160.7:c.12791C>A	ENSP00000340648.3:p.Ser4264Tyr
ENST00000426907.5:c.3258C>A
ENST00000488459.1:n.104C>A
ENST00000612484.4:c.12764C>A	ENSP00000479451.1:p.Ser4255Tyr
NM_031407.6:c.12791C>A	NP_113584.3:p.Ser4264Tyr
XM_005261965.2:c.12791C>A	XP_005262022.1:p.Ser4264Tyr
XM_011530746.1:c.13040C>A	XP_011529048.1:p.Ser4347Tyr
XM_011530747.1:c.13040C>A	XP_011529049.1:p.Ser4347Tyr
XM_011530748.1:c.13040C>A	XP_011529050.1:p.Ser4347Tyr
XM_011530749.1:c.13040C>A	XP_011529051.1:p.Ser4347Tyr
XM_011530750.1:c.13040C>A	XP_011529052.1:p.Ser4347Tyr
XM_011530751.1:c.13040C>A	XP_011529053.1:p.Ser4347Tyr
XM_011530752.1:c.13037C>A	XP_011529054.1:p.Ser4346Tyr
XM_011530753.1:c.12995C>A	XP_011529055.1:p.Ser4332Tyr
XM_011530754.1:c.12992C>A	XP_011529056.1:p.Ser4331Tyr
XM_011530755.1:c.12989C>A	XP_011529057.1:p.Ser4330Tyr
XM_011530756.1:c.12941C>A	XP_011529058.1:p.Ser4314Tyr
XM_011530757.1:c.12638C>A	XP_011529059.1:p.Ser4213Tyr
XM_005261965.4:c.12791C>A	XP_005262022.1:p.Ser4264Tyr
XM_011530751.2:c.13040C>A	XP_011529053.1:p.Ser4347Tyr
XM_017029191.1:c.13172C>A	XP_016884680.1:p.Ser4391Tyr
XM_017029192.1:c.13169C>A	XP_016884681.1:p.Ser4390Tyr
XM_017029193.1:c.13151C>A	XP_016884682.1:p.Ser4384Tyr
XM_017029194.1:c.13127C>A	XP_016884683.1:p.Ser4376Tyr
XM_017029195.1:c.13124C>A	XP_016884684.1:p.Ser4375Tyr
XM_017029196.1:c.13121C>A	XP_016884685.1:p.Ser4374Tyr
XM_017029197.1:c.13073C>A	XP_016884686.1:p.Ser4358Tyr
XM_017029198.2:c.13061C>A	XP_016884687.1:p.Ser4354Tyr
XM_017029199.1:c.13061C>A	XP_016884688.1:p.Ser4354Tyr
XM_017029200.1:c.13061C>A	XP_016884689.1:p.Ser4354Tyr
XM_017029201.1:c.13061C>A	XP_016884690.1:p.Ser4354Tyr
XM_017029202.1:c.13061C>A	XP_016884691.1:p.Ser4354Tyr
XM_017029203.1:c.13061C>A	XP_016884692.1:p.Ser4354Tyr
XM_017029204.1:c.12923C>A	XP_016884693.1:p.Ser4308Tyr
XM_017029206.1:c.12770C>A	XP_016884695.1:p.Ser4257Tyr
XM_024452322.1:c.13040C>A	XP_024308090.1:p.Ser4347Tyr
NM_031407.7:c.12791C>A MANE Select	NP_113584.3:p.Ser4264Tyr