Canonical Allele Identifier: CA516418259

Gene: HUWE1

Linked Data

• MyVariant Identifiers: chrX:g.53560988G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53534027G>T , CM000685.2:g.53534027G>T	GRCh38
NC_000023.10:g.53560988G>T , CM000685.1:g.53560988G>T	GRCh37
NC_000023.9:g.53577713G>T	NCBI36
NG_016261.2:g.157707C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704099.1:c.12786C>A	ENSP00000515693.1:p.Arg4262=
ENST00000262854.11:c.13002C>A MANE Select	ENSP00000262854.6:p.Arg4334=
ENST00000262854.10:c.13002C>A	ENSP00000262854.6:p.Arg4334=
ENST00000342160.7:c.13002C>A	ENSP00000340648.3:p.Arg4334=
ENST00000426907.5:c.3469C>A
ENST00000488459.1:n.315C>A
ENST00000612484.4:c.12975C>A	ENSP00000479451.1:p.Arg4325=
NM_031407.6:c.13002C>A	NP_113584.3:p.Arg4334=
XM_005261965.2:c.13002C>A	XP_005262022.1:p.Arg4334=
XM_011530746.1:c.13251C>A	XP_011529048.1:p.Arg4417=
XM_011530747.1:c.13251C>A	XP_011529049.1:p.Arg4417=
XM_011530748.1:c.13251C>A	XP_011529050.1:p.Arg4417=
XM_011530749.1:c.13251C>A	XP_011529051.1:p.Arg4417=
XM_011530750.1:c.13251C>A	XP_011529052.1:p.Arg4417=
XM_011530751.1:c.13251C>A	XP_011529053.1:p.Arg4417=
XM_011530752.1:c.13248C>A	XP_011529054.1:p.Arg4416=
XM_011530753.1:c.13206C>A	XP_011529055.1:p.Arg4402=
XM_011530754.1:c.13203C>A	XP_011529056.1:p.Arg4401=
XM_011530755.1:c.13200C>A	XP_011529057.1:p.Arg4400=
XM_011530756.1:c.13152C>A	XP_011529058.1:p.Arg4384=
XM_011530757.1:c.12849C>A	XP_011529059.1:p.Arg4283=
XM_005261965.4:c.13002C>A	XP_005262022.1:p.Arg4334=
XM_011530751.2:c.13251C>A	XP_011529053.1:p.Arg4417=
XM_017029191.1:c.13383C>A	XP_016884680.1:p.Arg4461=
XM_017029192.1:c.13380C>A	XP_016884681.1:p.Arg4460=
XM_017029193.1:c.13362C>A	XP_016884682.1:p.Arg4454=
XM_017029194.1:c.13338C>A	XP_016884683.1:p.Arg4446=
XM_017029195.1:c.13335C>A	XP_016884684.1:p.Arg4445=
XM_017029196.1:c.13332C>A	XP_016884685.1:p.Arg4444=
XM_017029197.1:c.13284C>A	XP_016884686.1:p.Arg4428=
XM_017029198.2:c.13272C>A	XP_016884687.1:p.Arg4424=
XM_017029199.1:c.13272C>A	XP_016884688.1:p.Arg4424=
XM_017029200.1:c.13272C>A	XP_016884689.1:p.Arg4424=
XM_017029201.1:c.13272C>A	XP_016884690.1:p.Arg4424=
XM_017029202.1:c.13272C>A	XP_016884691.1:p.Arg4424=
XM_017029203.1:c.13272C>A	XP_016884692.1:p.Arg4424=
XM_017029204.1:c.13134C>A	XP_016884693.1:p.Arg4378=
XM_017029206.1:c.12981C>A	XP_016884695.1:p.Arg4327=
XM_024452322.1:c.13251C>A	XP_024308090.1:p.Arg4417=
NM_031407.7:c.13002C>A MANE Select	NP_113584.3:p.Arg4334=