Canonical Allele Identifier: CA413145246

Gene: HUWE1

Linked Data

• MyVariant Identifiers: chrX:g.53561128A>G (hg19) ; chrX:g.53534167A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53534167A>G , CM000685.2:g.53534167A>G	GRCh38
NC_000023.10:g.53561128A>G , CM000685.1:g.53561128A>G	GRCh37
NC_000023.9:g.53577853A>G	NCBI36
NG_016261.2:g.157567T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704099.1:c.12646T>C	ENSP00000515693.1:p.Phe4216Leu
ENST00000262854.11:c.12862T>C MANE Select	ENSP00000262854.6:p.Phe4288Leu
ENST00000262854.10:c.12862T>C	ENSP00000262854.6:p.Phe4288Leu
ENST00000342160.7:c.12862T>C	ENSP00000340648.3:p.Phe4288Leu
ENST00000426907.5:c.3329T>C
ENST00000488459.1:n.175T>C
ENST00000612484.4:c.12835T>C	ENSP00000479451.1:p.Phe4279Leu
NM_031407.6:c.12862T>C	NP_113584.3:p.Phe4288Leu
XM_005261965.2:c.12862T>C	XP_005262022.1:p.Phe4288Leu
XM_011530746.1:c.13111T>C	XP_011529048.1:p.Phe4371Leu
XM_011530747.1:c.13111T>C	XP_011529049.1:p.Phe4371Leu
XM_011530748.1:c.13111T>C	XP_011529050.1:p.Phe4371Leu
XM_011530749.1:c.13111T>C	XP_011529051.1:p.Phe4371Leu
XM_011530750.1:c.13111T>C	XP_011529052.1:p.Phe4371Leu
XM_011530751.1:c.13111T>C	XP_011529053.1:p.Phe4371Leu
XM_011530752.1:c.13108T>C	XP_011529054.1:p.Phe4370Leu
XM_011530753.1:c.13066T>C	XP_011529055.1:p.Phe4356Leu
XM_011530754.1:c.13063T>C	XP_011529056.1:p.Phe4355Leu
XM_011530755.1:c.13060T>C	XP_011529057.1:p.Phe4354Leu
XM_011530756.1:c.13012T>C	XP_011529058.1:p.Phe4338Leu
XM_011530757.1:c.12709T>C	XP_011529059.1:p.Phe4237Leu
XM_005261965.4:c.12862T>C	XP_005262022.1:p.Phe4288Leu
XM_011530751.2:c.13111T>C	XP_011529053.1:p.Phe4371Leu
XM_017029191.1:c.13243T>C	XP_016884680.1:p.Phe4415Leu
XM_017029192.1:c.13240T>C	XP_016884681.1:p.Phe4414Leu
XM_017029193.1:c.13222T>C	XP_016884682.1:p.Phe4408Leu
XM_017029194.1:c.13198T>C	XP_016884683.1:p.Phe4400Leu
XM_017029195.1:c.13195T>C	XP_016884684.1:p.Phe4399Leu
XM_017029196.1:c.13192T>C	XP_016884685.1:p.Phe4398Leu
XM_017029197.1:c.13144T>C	XP_016884686.1:p.Phe4382Leu
XM_017029198.2:c.13132T>C	XP_016884687.1:p.Phe4378Leu
XM_017029199.1:c.13132T>C	XP_016884688.1:p.Phe4378Leu
XM_017029200.1:c.13132T>C	XP_016884689.1:p.Phe4378Leu
XM_017029201.1:c.13132T>C	XP_016884690.1:p.Phe4378Leu
XM_017029202.1:c.13132T>C	XP_016884691.1:p.Phe4378Leu
XM_017029203.1:c.13132T>C	XP_016884692.1:p.Phe4378Leu
XM_017029204.1:c.12994T>C	XP_016884693.1:p.Phe4332Leu
XM_017029206.1:c.12841T>C	XP_016884695.1:p.Phe4281Leu
XM_024452322.1:c.13111T>C	XP_024308090.1:p.Phe4371Leu
NM_031407.7:c.12862T>C MANE Select	NP_113584.3:p.Phe4288Leu