Canonical Allele Identifier: CA413146154

Gene: HUWE1

Linked Data

• MyVariant Identifiers: chrX:g.53561524G>T (hg19) ; chrX:g.53534563G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53534563G>T , CM000685.2:g.53534563G>T	GRCh38
NC_000023.10:g.53561524G>T , CM000685.1:g.53561524G>T	GRCh37
NC_000023.9:g.53578249G>T	NCBI36
NG_016261.2:g.157171C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704099.1:c.12568C>A	ENSP00000515693.1:p.Leu4190Met
ENST00000262854.11:c.12784C>A MANE Select	ENSP00000262854.6:p.Leu4262Met
ENST00000262854.10:c.12784C>A	ENSP00000262854.6:p.Leu4262Met
ENST00000342160.7:c.12784C>A	ENSP00000340648.3:p.Leu4262Met
ENST00000426907.5:c.3251C>A
ENST00000488459.1:n.97C>A
ENST00000612484.4:c.12757C>A	ENSP00000479451.1:p.Leu4253Met
NM_031407.6:c.12784C>A	NP_113584.3:p.Leu4262Met
XM_005261965.2:c.12784C>A	XP_005262022.1:p.Leu4262Met
XM_011530746.1:c.13033C>A	XP_011529048.1:p.Leu4345Met
XM_011530747.1:c.13033C>A	XP_011529049.1:p.Leu4345Met
XM_011530748.1:c.13033C>A	XP_011529050.1:p.Leu4345Met
XM_011530749.1:c.13033C>A	XP_011529051.1:p.Leu4345Met
XM_011530750.1:c.13033C>A	XP_011529052.1:p.Leu4345Met
XM_011530751.1:c.13033C>A	XP_011529053.1:p.Leu4345Met
XM_011530752.1:c.13030C>A	XP_011529054.1:p.Leu4344Met
XM_011530753.1:c.12988C>A	XP_011529055.1:p.Leu4330Met
XM_011530754.1:c.12985C>A	XP_011529056.1:p.Leu4329Met
XM_011530755.1:c.12982C>A	XP_011529057.1:p.Leu4328Met
XM_011530756.1:c.12934C>A	XP_011529058.1:p.Leu4312Met
XM_011530757.1:c.12631C>A	XP_011529059.1:p.Leu4211Met
XM_005261965.4:c.12784C>A	XP_005262022.1:p.Leu4262Met
XM_011530751.2:c.13033C>A	XP_011529053.1:p.Leu4345Met
XM_017029191.1:c.13165C>A	XP_016884680.1:p.Leu4389Met
XM_017029192.1:c.13162C>A	XP_016884681.1:p.Leu4388Met
XM_017029193.1:c.13144C>A	XP_016884682.1:p.Leu4382Met
XM_017029194.1:c.13120C>A	XP_016884683.1:p.Leu4374Met
XM_017029195.1:c.13117C>A	XP_016884684.1:p.Leu4373Met
XM_017029196.1:c.13114C>A	XP_016884685.1:p.Leu4372Met
XM_017029197.1:c.13066C>A	XP_016884686.1:p.Leu4356Met
XM_017029198.2:c.13054C>A	XP_016884687.1:p.Leu4352Met
XM_017029199.1:c.13054C>A	XP_016884688.1:p.Leu4352Met
XM_017029200.1:c.13054C>A	XP_016884689.1:p.Leu4352Met
XM_017029201.1:c.13054C>A	XP_016884690.1:p.Leu4352Met
XM_017029202.1:c.13054C>A	XP_016884691.1:p.Leu4352Met
XM_017029203.1:c.13054C>A	XP_016884692.1:p.Leu4352Met
XM_017029204.1:c.12916C>A	XP_016884693.1:p.Leu4306Met
XM_017029206.1:c.12763C>A	XP_016884695.1:p.Leu4255Met
XM_024452322.1:c.13033C>A	XP_024308090.1:p.Leu4345Met
NM_031407.7:c.12784C>A MANE Select	NP_113584.3:p.Leu4262Met