Canonical Allele Identifier: CA413144869

Gene: HUWE1

Linked Data

• MyVariant Identifiers: chrX:g.53561104A>C (hg19) ; chrX:g.53534143A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53534143A>C , CM000685.2:g.53534143A>C	GRCh38
NC_000023.10:g.53561104A>C , CM000685.1:g.53561104A>C	GRCh37
NC_000023.9:g.53577829A>C	NCBI36
NG_016261.2:g.157591T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704099.1:c.12670T>G	ENSP00000515693.1:p.Phe4224Val
ENST00000262854.11:c.12886T>G MANE Select	ENSP00000262854.6:p.Phe4296Val
ENST00000262854.10:c.12886T>G	ENSP00000262854.6:p.Phe4296Val
ENST00000342160.7:c.12886T>G	ENSP00000340648.3:p.Phe4296Val
ENST00000426907.5:c.3353T>G
ENST00000488459.1:n.199T>G
ENST00000612484.4:c.12859T>G	ENSP00000479451.1:p.Phe4287Val
NM_031407.6:c.12886T>G	NP_113584.3:p.Phe4296Val
XM_005261965.2:c.12886T>G	XP_005262022.1:p.Phe4296Val
XM_011530746.1:c.13135T>G	XP_011529048.1:p.Phe4379Val
XM_011530747.1:c.13135T>G	XP_011529049.1:p.Phe4379Val
XM_011530748.1:c.13135T>G	XP_011529050.1:p.Phe4379Val
XM_011530749.1:c.13135T>G	XP_011529051.1:p.Phe4379Val
XM_011530750.1:c.13135T>G	XP_011529052.1:p.Phe4379Val
XM_011530751.1:c.13135T>G	XP_011529053.1:p.Phe4379Val
XM_011530752.1:c.13132T>G	XP_011529054.1:p.Phe4378Val
XM_011530753.1:c.13090T>G	XP_011529055.1:p.Phe4364Val
XM_011530754.1:c.13087T>G	XP_011529056.1:p.Phe4363Val
XM_011530755.1:c.13084T>G	XP_011529057.1:p.Phe4362Val
XM_011530756.1:c.13036T>G	XP_011529058.1:p.Phe4346Val
XM_011530757.1:c.12733T>G	XP_011529059.1:p.Phe4245Val
XM_005261965.4:c.12886T>G	XP_005262022.1:p.Phe4296Val
XM_011530751.2:c.13135T>G	XP_011529053.1:p.Phe4379Val
XM_017029191.1:c.13267T>G	XP_016884680.1:p.Phe4423Val
XM_017029192.1:c.13264T>G	XP_016884681.1:p.Phe4422Val
XM_017029193.1:c.13246T>G	XP_016884682.1:p.Phe4416Val
XM_017029194.1:c.13222T>G	XP_016884683.1:p.Phe4408Val
XM_017029195.1:c.13219T>G	XP_016884684.1:p.Phe4407Val
XM_017029196.1:c.13216T>G	XP_016884685.1:p.Phe4406Val
XM_017029197.1:c.13168T>G	XP_016884686.1:p.Phe4390Val
XM_017029198.2:c.13156T>G	XP_016884687.1:p.Phe4386Val
XM_017029199.1:c.13156T>G	XP_016884688.1:p.Phe4386Val
XM_017029200.1:c.13156T>G	XP_016884689.1:p.Phe4386Val
XM_017029201.1:c.13156T>G	XP_016884690.1:p.Phe4386Val
XM_017029202.1:c.13156T>G	XP_016884691.1:p.Phe4386Val
XM_017029203.1:c.13156T>G	XP_016884692.1:p.Phe4386Val
XM_017029204.1:c.13018T>G	XP_016884693.1:p.Phe4340Val
XM_017029206.1:c.12865T>G	XP_016884695.1:p.Phe4289Val
XM_024452322.1:c.13135T>G	XP_024308090.1:p.Phe4379Val
NM_031407.7:c.12886T>G MANE Select	NP_113584.3:p.Phe4296Val