Canonical Allele Identifier: CA413145072

Gene: HUWE1

Linked Data

• gnomAD v4: X-53534157-G-T
• MyVariant Identifiers: chrX:g.53561118G>T (hg19) ; chrX:g.53534157G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53534157G>T , CM000685.2:g.53534157G>T	GRCh38
NC_000023.10:g.53561118G>T , CM000685.1:g.53561118G>T	GRCh37
NC_000023.9:g.53577843G>T	NCBI36
NG_016261.2:g.157577C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704099.1:c.12656C>A	ENSP00000515693.1:p.Ala4219Asp
ENST00000262854.11:c.12872C>A MANE Select	ENSP00000262854.6:p.Ala4291Asp
ENST00000262854.10:c.12872C>A	ENSP00000262854.6:p.Ala4291Asp
ENST00000342160.7:c.12872C>A	ENSP00000340648.3:p.Ala4291Asp
ENST00000426907.5:c.3339C>A
ENST00000488459.1:n.185C>A
ENST00000612484.4:c.12845C>A	ENSP00000479451.1:p.Ala4282Asp
NM_031407.6:c.12872C>A	NP_113584.3:p.Ala4291Asp
XM_005261965.2:c.12872C>A	XP_005262022.1:p.Ala4291Asp
XM_011530746.1:c.13121C>A	XP_011529048.1:p.Ala4374Asp
XM_011530747.1:c.13121C>A	XP_011529049.1:p.Ala4374Asp
XM_011530748.1:c.13121C>A	XP_011529050.1:p.Ala4374Asp
XM_011530749.1:c.13121C>A	XP_011529051.1:p.Ala4374Asp
XM_011530750.1:c.13121C>A	XP_011529052.1:p.Ala4374Asp
XM_011530751.1:c.13121C>A	XP_011529053.1:p.Ala4374Asp
XM_011530752.1:c.13118C>A	XP_011529054.1:p.Ala4373Asp
XM_011530753.1:c.13076C>A	XP_011529055.1:p.Ala4359Asp
XM_011530754.1:c.13073C>A	XP_011529056.1:p.Ala4358Asp
XM_011530755.1:c.13070C>A	XP_011529057.1:p.Ala4357Asp
XM_011530756.1:c.13022C>A	XP_011529058.1:p.Ala4341Asp
XM_011530757.1:c.12719C>A	XP_011529059.1:p.Ala4240Asp
XM_005261965.4:c.12872C>A	XP_005262022.1:p.Ala4291Asp
XM_011530751.2:c.13121C>A	XP_011529053.1:p.Ala4374Asp
XM_017029191.1:c.13253C>A	XP_016884680.1:p.Ala4418Asp
XM_017029192.1:c.13250C>A	XP_016884681.1:p.Ala4417Asp
XM_017029193.1:c.13232C>A	XP_016884682.1:p.Ala4411Asp
XM_017029194.1:c.13208C>A	XP_016884683.1:p.Ala4403Asp
XM_017029195.1:c.13205C>A	XP_016884684.1:p.Ala4402Asp
XM_017029196.1:c.13202C>A	XP_016884685.1:p.Ala4401Asp
XM_017029197.1:c.13154C>A	XP_016884686.1:p.Ala4385Asp
XM_017029198.2:c.13142C>A	XP_016884687.1:p.Ala4381Asp
XM_017029199.1:c.13142C>A	XP_016884688.1:p.Ala4381Asp
XM_017029200.1:c.13142C>A	XP_016884689.1:p.Ala4381Asp
XM_017029201.1:c.13142C>A	XP_016884690.1:p.Ala4381Asp
XM_017029202.1:c.13142C>A	XP_016884691.1:p.Ala4381Asp
XM_017029203.1:c.13142C>A	XP_016884692.1:p.Ala4381Asp
XM_017029204.1:c.13004C>A	XP_016884693.1:p.Ala4335Asp
XM_017029206.1:c.12851C>A	XP_016884695.1:p.Ala4284Asp
XM_024452322.1:c.13121C>A	XP_024308090.1:p.Ala4374Asp
NM_031407.7:c.12872C>A MANE Select	NP_113584.3:p.Ala4291Asp