Canonical Allele Identifier: CA413145214

Gene: HUWE1

Linked Data

• MyVariant Identifiers: chrX:g.53561127A>G (hg19) ; chrX:g.53534166A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53534166A>G , CM000685.2:g.53534166A>G	GRCh38
NC_000023.10:g.53561127A>G , CM000685.1:g.53561127A>G	GRCh37
NC_000023.9:g.53577852A>G	NCBI36
NG_016261.2:g.157568T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704099.1:c.12647T>C	ENSP00000515693.1:p.Phe4216Ser
ENST00000262854.11:c.12863T>C MANE Select	ENSP00000262854.6:p.Phe4288Ser
ENST00000262854.10:c.12863T>C	ENSP00000262854.6:p.Phe4288Ser
ENST00000342160.7:c.12863T>C	ENSP00000340648.3:p.Phe4288Ser
ENST00000426907.5:c.3330T>C
ENST00000488459.1:n.176T>C
ENST00000612484.4:c.12836T>C	ENSP00000479451.1:p.Phe4279Ser
NM_031407.6:c.12863T>C	NP_113584.3:p.Phe4288Ser
XM_005261965.2:c.12863T>C	XP_005262022.1:p.Phe4288Ser
XM_011530746.1:c.13112T>C	XP_011529048.1:p.Phe4371Ser
XM_011530747.1:c.13112T>C	XP_011529049.1:p.Phe4371Ser
XM_011530748.1:c.13112T>C	XP_011529050.1:p.Phe4371Ser
XM_011530749.1:c.13112T>C	XP_011529051.1:p.Phe4371Ser
XM_011530750.1:c.13112T>C	XP_011529052.1:p.Phe4371Ser
XM_011530751.1:c.13112T>C	XP_011529053.1:p.Phe4371Ser
XM_011530752.1:c.13109T>C	XP_011529054.1:p.Phe4370Ser
XM_011530753.1:c.13067T>C	XP_011529055.1:p.Phe4356Ser
XM_011530754.1:c.13064T>C	XP_011529056.1:p.Phe4355Ser
XM_011530755.1:c.13061T>C	XP_011529057.1:p.Phe4354Ser
XM_011530756.1:c.13013T>C	XP_011529058.1:p.Phe4338Ser
XM_011530757.1:c.12710T>C	XP_011529059.1:p.Phe4237Ser
XM_005261965.4:c.12863T>C	XP_005262022.1:p.Phe4288Ser
XM_011530751.2:c.13112T>C	XP_011529053.1:p.Phe4371Ser
XM_017029191.1:c.13244T>C	XP_016884680.1:p.Phe4415Ser
XM_017029192.1:c.13241T>C	XP_016884681.1:p.Phe4414Ser
XM_017029193.1:c.13223T>C	XP_016884682.1:p.Phe4408Ser
XM_017029194.1:c.13199T>C	XP_016884683.1:p.Phe4400Ser
XM_017029195.1:c.13196T>C	XP_016884684.1:p.Phe4399Ser
XM_017029196.1:c.13193T>C	XP_016884685.1:p.Phe4398Ser
XM_017029197.1:c.13145T>C	XP_016884686.1:p.Phe4382Ser
XM_017029198.2:c.13133T>C	XP_016884687.1:p.Phe4378Ser
XM_017029199.1:c.13133T>C	XP_016884688.1:p.Phe4378Ser
XM_017029200.1:c.13133T>C	XP_016884689.1:p.Phe4378Ser
XM_017029201.1:c.13133T>C	XP_016884690.1:p.Phe4378Ser
XM_017029202.1:c.13133T>C	XP_016884691.1:p.Phe4378Ser
XM_017029203.1:c.13133T>C	XP_016884692.1:p.Phe4378Ser
XM_017029204.1:c.12995T>C	XP_016884693.1:p.Phe4332Ser
XM_017029206.1:c.12842T>C	XP_016884695.1:p.Phe4281Ser
XM_024452322.1:c.13112T>C	XP_024308090.1:p.Phe4371Ser
NM_031407.7:c.12863T>C MANE Select	NP_113584.3:p.Phe4288Ser