Canonical Allele Identifier: CA413144982

Gene: HUWE1

Linked Data

• MyVariant Identifiers: chrX:g.53561112C>G (hg19) ; chrX:g.53534151C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53534151C>G , CM000685.2:g.53534151C>G	GRCh38
NC_000023.10:g.53561112C>G , CM000685.1:g.53561112C>G	GRCh37
NC_000023.9:g.53577837C>G	NCBI36
NG_016261.2:g.157583G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704099.1:c.12662G>C	ENSP00000515693.1:p.Arg4221Pro
ENST00000262854.11:c.12878G>C MANE Select	ENSP00000262854.6:p.Arg4293Pro
ENST00000262854.10:c.12878G>C	ENSP00000262854.6:p.Arg4293Pro
ENST00000342160.7:c.12878G>C	ENSP00000340648.3:p.Arg4293Pro
ENST00000426907.5:c.3345G>C
ENST00000488459.1:n.191G>C
ENST00000612484.4:c.12851G>C	ENSP00000479451.1:p.Arg4284Pro
NM_031407.6:c.12878G>C	NP_113584.3:p.Arg4293Pro
XM_005261965.2:c.12878G>C	XP_005262022.1:p.Arg4293Pro
XM_011530746.1:c.13127G>C	XP_011529048.1:p.Arg4376Pro
XM_011530747.1:c.13127G>C	XP_011529049.1:p.Arg4376Pro
XM_011530748.1:c.13127G>C	XP_011529050.1:p.Arg4376Pro
XM_011530749.1:c.13127G>C	XP_011529051.1:p.Arg4376Pro
XM_011530750.1:c.13127G>C	XP_011529052.1:p.Arg4376Pro
XM_011530751.1:c.13127G>C	XP_011529053.1:p.Arg4376Pro
XM_011530752.1:c.13124G>C	XP_011529054.1:p.Arg4375Pro
XM_011530753.1:c.13082G>C	XP_011529055.1:p.Arg4361Pro
XM_011530754.1:c.13079G>C	XP_011529056.1:p.Arg4360Pro
XM_011530755.1:c.13076G>C	XP_011529057.1:p.Arg4359Pro
XM_011530756.1:c.13028G>C	XP_011529058.1:p.Arg4343Pro
XM_011530757.1:c.12725G>C	XP_011529059.1:p.Arg4242Pro
XM_005261965.4:c.12878G>C	XP_005262022.1:p.Arg4293Pro
XM_011530751.2:c.13127G>C	XP_011529053.1:p.Arg4376Pro
XM_017029191.1:c.13259G>C	XP_016884680.1:p.Arg4420Pro
XM_017029192.1:c.13256G>C	XP_016884681.1:p.Arg4419Pro
XM_017029193.1:c.13238G>C	XP_016884682.1:p.Arg4413Pro
XM_017029194.1:c.13214G>C	XP_016884683.1:p.Arg4405Pro
XM_017029195.1:c.13211G>C	XP_016884684.1:p.Arg4404Pro
XM_017029196.1:c.13208G>C	XP_016884685.1:p.Arg4403Pro
XM_017029197.1:c.13160G>C	XP_016884686.1:p.Arg4387Pro
XM_017029198.2:c.13148G>C	XP_016884687.1:p.Arg4383Pro
XM_017029199.1:c.13148G>C	XP_016884688.1:p.Arg4383Pro
XM_017029200.1:c.13148G>C	XP_016884689.1:p.Arg4383Pro
XM_017029201.1:c.13148G>C	XP_016884690.1:p.Arg4383Pro
XM_017029202.1:c.13148G>C	XP_016884691.1:p.Arg4383Pro
XM_017029203.1:c.13148G>C	XP_016884692.1:p.Arg4383Pro
XM_017029204.1:c.13010G>C	XP_016884693.1:p.Arg4337Pro
XM_017029206.1:c.12857G>C	XP_016884695.1:p.Arg4286Pro
XM_024452322.1:c.13127G>C	XP_024308090.1:p.Arg4376Pro
NM_031407.7:c.12878G>C MANE Select	NP_113584.3:p.Arg4293Pro