Canonical Allele Identifier: CA413155615

Gene: HUWE1

Linked Data

• MyVariant Identifiers: chrX:g.53564601G>C (hg19) ; chrX:g.53537640G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53537640G>C , CM000685.2:g.53537640G>C	GRCh38
NC_000023.10:g.53564601G>C , CM000685.1:g.53564601G>C	GRCh37
NC_000023.9:g.53581326G>C	NCBI36
NG_016261.2:g.154094C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704099.1:c.11837C>G	ENSP00000515693.1:p.Ala3946Gly
ENST00000262854.11:c.12053C>G MANE Select	ENSP00000262854.6:p.Ala4018Gly
ENST00000262854.10:c.12053C>G	ENSP00000262854.6:p.Ala4018Gly
ENST00000342160.7:c.12053C>G	ENSP00000340648.3:p.Ala4018Gly
ENST00000426907.5:c.2520C>G
ENST00000480438.1:n.188C>G
ENST00000612484.4:c.12026C>G	ENSP00000479451.1:p.Ala4009Gly
NM_031407.6:c.12053C>G	NP_113584.3:p.Ala4018Gly
XM_005261965.2:c.12053C>G	XP_005262022.1:p.Ala4018Gly
XM_011530746.1:c.12302C>G	XP_011529048.1:p.Ala4101Gly
XM_011530747.1:c.12302C>G	XP_011529049.1:p.Ala4101Gly
XM_011530748.1:c.12302C>G	XP_011529050.1:p.Ala4101Gly
XM_011530749.1:c.12302C>G	XP_011529051.1:p.Ala4101Gly
XM_011530750.1:c.12302C>G	XP_011529052.1:p.Ala4101Gly
XM_011530751.1:c.12302C>G	XP_011529053.1:p.Ala4101Gly
XM_011530752.1:c.12299C>G	XP_011529054.1:p.Ala4100Gly
XM_011530753.1:c.12257C>G	XP_011529055.1:p.Ala4086Gly
XM_011530754.1:c.12254C>G	XP_011529056.1:p.Ala4085Gly
XM_011530755.1:c.12251C>G	XP_011529057.1:p.Ala4084Gly
XM_011530756.1:c.12203C>G	XP_011529058.1:p.Ala4068Gly
XM_011530757.1:c.11900C>G	XP_011529059.1:p.Ala3967Gly
XM_005261965.4:c.12053C>G	XP_005262022.1:p.Ala4018Gly
XM_011530751.2:c.12302C>G	XP_011529053.1:p.Ala4101Gly
XM_017029191.1:c.12434C>G	XP_016884680.1:p.Ala4145Gly
XM_017029192.1:c.12431C>G	XP_016884681.1:p.Ala4144Gly
XM_017029193.1:c.12413C>G	XP_016884682.1:p.Ala4138Gly
XM_017029194.1:c.12389C>G	XP_016884683.1:p.Ala4130Gly
XM_017029195.1:c.12386C>G	XP_016884684.1:p.Ala4129Gly
XM_017029196.1:c.12383C>G	XP_016884685.1:p.Ala4128Gly
XM_017029197.1:c.12335C>G	XP_016884686.1:p.Ala4112Gly
XM_017029198.2:c.12323C>G	XP_016884687.1:p.Ala4108Gly
XM_017029199.1:c.12323C>G	XP_016884688.1:p.Ala4108Gly
XM_017029200.1:c.12323C>G	XP_016884689.1:p.Ala4108Gly
XM_017029201.1:c.12323C>G	XP_016884690.1:p.Ala4108Gly
XM_017029202.1:c.12323C>G	XP_016884691.1:p.Ala4108Gly
XM_017029203.1:c.12323C>G	XP_016884692.1:p.Ala4108Gly
XM_017029204.1:c.12185C>G	XP_016884693.1:p.Ala4062Gly
XM_017029206.1:c.12032C>G	XP_016884695.1:p.Ala4011Gly
XM_024452322.1:c.12302C>G	XP_024308090.1:p.Ala4101Gly
NM_031407.7:c.12053C>G MANE Select	NP_113584.3:p.Ala4018Gly