Canonical Allele Identifier: CA516418655

Gene: HUWE1

Linked Data

• MyVariant Identifiers: chrX:g.53561033G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53534072G>T , CM000685.2:g.53534072G>T	GRCh38
NC_000023.10:g.53561033G>T , CM000685.1:g.53561033G>T	GRCh37
NC_000023.9:g.53577758G>T	NCBI36
NG_016261.2:g.157662C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704099.1:c.12741C>A	ENSP00000515693.1:p.Gly4247=
ENST00000262854.11:c.12957C>A MANE Select	ENSP00000262854.6:p.Gly4319=
ENST00000262854.10:c.12957C>A	ENSP00000262854.6:p.Gly4319=
ENST00000342160.7:c.12957C>A	ENSP00000340648.3:p.Gly4319=
ENST00000426907.5:c.3424C>A
ENST00000488459.1:n.270C>A
ENST00000612484.4:c.12930C>A	ENSP00000479451.1:p.Gly4310=
NM_031407.6:c.12957C>A	NP_113584.3:p.Gly4319=
XM_005261965.2:c.12957C>A	XP_005262022.1:p.Gly4319=
XM_011530746.1:c.13206C>A	XP_011529048.1:p.Gly4402=
XM_011530747.1:c.13206C>A	XP_011529049.1:p.Gly4402=
XM_011530748.1:c.13206C>A	XP_011529050.1:p.Gly4402=
XM_011530749.1:c.13206C>A	XP_011529051.1:p.Gly4402=
XM_011530750.1:c.13206C>A	XP_011529052.1:p.Gly4402=
XM_011530751.1:c.13206C>A	XP_011529053.1:p.Gly4402=
XM_011530752.1:c.13203C>A	XP_011529054.1:p.Gly4401=
XM_011530753.1:c.13161C>A	XP_011529055.1:p.Gly4387=
XM_011530754.1:c.13158C>A	XP_011529056.1:p.Gly4386=
XM_011530755.1:c.13155C>A	XP_011529057.1:p.Gly4385=
XM_011530756.1:c.13107C>A	XP_011529058.1:p.Gly4369=
XM_011530757.1:c.12804C>A	XP_011529059.1:p.Gly4268=
XM_005261965.4:c.12957C>A	XP_005262022.1:p.Gly4319=
XM_011530751.2:c.13206C>A	XP_011529053.1:p.Gly4402=
XM_017029191.1:c.13338C>A	XP_016884680.1:p.Gly4446=
XM_017029192.1:c.13335C>A	XP_016884681.1:p.Gly4445=
XM_017029193.1:c.13317C>A	XP_016884682.1:p.Gly4439=
XM_017029194.1:c.13293C>A	XP_016884683.1:p.Gly4431=
XM_017029195.1:c.13290C>A	XP_016884684.1:p.Gly4430=
XM_017029196.1:c.13287C>A	XP_016884685.1:p.Gly4429=
XM_017029197.1:c.13239C>A	XP_016884686.1:p.Gly4413=
XM_017029198.2:c.13227C>A	XP_016884687.1:p.Gly4409=
XM_017029199.1:c.13227C>A	XP_016884688.1:p.Gly4409=
XM_017029200.1:c.13227C>A	XP_016884689.1:p.Gly4409=
XM_017029201.1:c.13227C>A	XP_016884690.1:p.Gly4409=
XM_017029202.1:c.13227C>A	XP_016884691.1:p.Gly4409=
XM_017029203.1:c.13227C>A	XP_016884692.1:p.Gly4409=
XM_017029204.1:c.13089C>A	XP_016884693.1:p.Gly4363=
XM_017029206.1:c.12936C>A	XP_016884695.1:p.Gly4312=
XM_024452322.1:c.13206C>A	XP_024308090.1:p.Gly4402=
NM_031407.7:c.12957C>A MANE Select	NP_113584.3:p.Gly4319=