Canonical Allele Identifier: CA413146859

Gene: HUWE1

Linked Data

• MyVariant Identifiers: chrX:g.53561611T>G (hg19) ; chrX:g.53534650T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53534650T>G , CM000685.2:g.53534650T>G	GRCh38
NC_000023.10:g.53561611T>G , CM000685.1:g.53561611T>G	GRCh37
NC_000023.9:g.53578336T>G	NCBI36
NG_016261.2:g.157084A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704099.1:c.12481A>C	ENSP00000515693.1:p.Ile4161Leu
ENST00000262854.11:c.12697A>C MANE Select	ENSP00000262854.6:p.Ile4233Leu
ENST00000262854.10:c.12697A>C	ENSP00000262854.6:p.Ile4233Leu
ENST00000342160.7:c.12697A>C	ENSP00000340648.3:p.Ile4233Leu
ENST00000426907.5:c.3164A>C
ENST00000488459.1:n.10A>C
ENST00000612484.4:c.12670A>C	ENSP00000479451.1:p.Ile4224Leu
NM_031407.6:c.12697A>C	NP_113584.3:p.Ile4233Leu
XM_005261965.2:c.12697A>C	XP_005262022.1:p.Ile4233Leu
XM_011530746.1:c.12946A>C	XP_011529048.1:p.Ile4316Leu
XM_011530747.1:c.12946A>C	XP_011529049.1:p.Ile4316Leu
XM_011530748.1:c.12946A>C	XP_011529050.1:p.Ile4316Leu
XM_011530749.1:c.12946A>C	XP_011529051.1:p.Ile4316Leu
XM_011530750.1:c.12946A>C	XP_011529052.1:p.Ile4316Leu
XM_011530751.1:c.12946A>C	XP_011529053.1:p.Ile4316Leu
XM_011530752.1:c.12943A>C	XP_011529054.1:p.Ile4315Leu
XM_011530753.1:c.12901A>C	XP_011529055.1:p.Ile4301Leu
XM_011530754.1:c.12898A>C	XP_011529056.1:p.Ile4300Leu
XM_011530755.1:c.12895A>C	XP_011529057.1:p.Ile4299Leu
XM_011530756.1:c.12847A>C	XP_011529058.1:p.Ile4283Leu
XM_011530757.1:c.12544A>C	XP_011529059.1:p.Ile4182Leu
XM_005261965.4:c.12697A>C	XP_005262022.1:p.Ile4233Leu
XM_011530751.2:c.12946A>C	XP_011529053.1:p.Ile4316Leu
XM_017029191.1:c.13078A>C	XP_016884680.1:p.Ile4360Leu
XM_017029192.1:c.13075A>C	XP_016884681.1:p.Ile4359Leu
XM_017029193.1:c.13057A>C	XP_016884682.1:p.Ile4353Leu
XM_017029194.1:c.13033A>C	XP_016884683.1:p.Ile4345Leu
XM_017029195.1:c.13030A>C	XP_016884684.1:p.Ile4344Leu
XM_017029196.1:c.13027A>C	XP_016884685.1:p.Ile4343Leu
XM_017029197.1:c.12979A>C	XP_016884686.1:p.Ile4327Leu
XM_017029198.2:c.12967A>C	XP_016884687.1:p.Ile4323Leu
XM_017029199.1:c.12967A>C	XP_016884688.1:p.Ile4323Leu
XM_017029200.1:c.12967A>C	XP_016884689.1:p.Ile4323Leu
XM_017029201.1:c.12967A>C	XP_016884690.1:p.Ile4323Leu
XM_017029202.1:c.12967A>C	XP_016884691.1:p.Ile4323Leu
XM_017029203.1:c.12967A>C	XP_016884692.1:p.Ile4323Leu
XM_017029204.1:c.12829A>C	XP_016884693.1:p.Ile4277Leu
XM_017029206.1:c.12676A>C	XP_016884695.1:p.Ile4226Leu
XM_024452322.1:c.12946A>C	XP_024308090.1:p.Ile4316Leu
NM_031407.7:c.12697A>C MANE Select	NP_113584.3:p.Ile4233Leu