Canonical Allele Identifier: CA413143562

Gene: HUWE1

Linked Data

• MyVariant Identifiers: chrX:g.53560981A>C (hg19) ; chrX:g.53534020A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53534020A>C , CM000685.2:g.53534020A>C	GRCh38
NC_000023.10:g.53560981A>C , CM000685.1:g.53560981A>C	GRCh37
NC_000023.9:g.53577706A>C	NCBI36
NG_016261.2:g.157714T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704099.1:c.12793T>G	ENSP00000515693.1:p.Ser4265Ala
ENST00000262854.11:c.13009T>G MANE Select	ENSP00000262854.6:p.Ser4337Ala
ENST00000262854.10:c.13009T>G	ENSP00000262854.6:p.Ser4337Ala
ENST00000342160.7:c.13009T>G	ENSP00000340648.3:p.Ser4337Ala
ENST00000426907.5:c.3476T>G
ENST00000488459.1:n.322T>G
ENST00000612484.4:c.12982T>G	ENSP00000479451.1:p.Ser4328Ala
NM_031407.6:c.13009T>G	NP_113584.3:p.Ser4337Ala
XM_005261965.2:c.13009T>G	XP_005262022.1:p.Ser4337Ala
XM_011530746.1:c.13258T>G	XP_011529048.1:p.Ser4420Ala
XM_011530747.1:c.13258T>G	XP_011529049.1:p.Ser4420Ala
XM_011530748.1:c.13258T>G	XP_011529050.1:p.Ser4420Ala
XM_011530749.1:c.13258T>G	XP_011529051.1:p.Ser4420Ala
XM_011530750.1:c.13258T>G	XP_011529052.1:p.Ser4420Ala
XM_011530751.1:c.13258T>G	XP_011529053.1:p.Ser4420Ala
XM_011530752.1:c.13255T>G	XP_011529054.1:p.Ser4419Ala
XM_011530753.1:c.13213T>G	XP_011529055.1:p.Ser4405Ala
XM_011530754.1:c.13210T>G	XP_011529056.1:p.Ser4404Ala
XM_011530755.1:c.13207T>G	XP_011529057.1:p.Ser4403Ala
XM_011530756.1:c.13159T>G	XP_011529058.1:p.Ser4387Ala
XM_011530757.1:c.12856T>G	XP_011529059.1:p.Ser4286Ala
XM_005261965.4:c.13009T>G	XP_005262022.1:p.Ser4337Ala
XM_011530751.2:c.13258T>G	XP_011529053.1:p.Ser4420Ala
XM_017029191.1:c.13390T>G	XP_016884680.1:p.Ser4464Ala
XM_017029192.1:c.13387T>G	XP_016884681.1:p.Ser4463Ala
XM_017029193.1:c.13369T>G	XP_016884682.1:p.Ser4457Ala
XM_017029194.1:c.13345T>G	XP_016884683.1:p.Ser4449Ala
XM_017029195.1:c.13342T>G	XP_016884684.1:p.Ser4448Ala
XM_017029196.1:c.13339T>G	XP_016884685.1:p.Ser4447Ala
XM_017029197.1:c.13291T>G	XP_016884686.1:p.Ser4431Ala
XM_017029198.2:c.13279T>G	XP_016884687.1:p.Ser4427Ala
XM_017029199.1:c.13279T>G	XP_016884688.1:p.Ser4427Ala
XM_017029200.1:c.13279T>G	XP_016884689.1:p.Ser4427Ala
XM_017029201.1:c.13279T>G	XP_016884690.1:p.Ser4427Ala
XM_017029202.1:c.13279T>G	XP_016884691.1:p.Ser4427Ala
XM_017029203.1:c.13279T>G	XP_016884692.1:p.Ser4427Ala
XM_017029204.1:c.13141T>G	XP_016884693.1:p.Ser4381Ala
XM_017029206.1:c.12988T>G	XP_016884695.1:p.Ser4330Ala
XM_024452322.1:c.13258T>G	XP_024308090.1:p.Ser4420Ala
NM_031407.7:c.13009T>G MANE Select	NP_113584.3:p.Ser4337Ala