Canonical Allele Identifier: CA413156147

Gene: HUWE1

Linked Data

• MyVariant Identifiers: chrX:g.53564647G>A (hg19) ; chrX:g.53537686G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53537686G>A , CM000685.2:g.53537686G>A	GRCh38
NC_000023.10:g.53564647G>A , CM000685.1:g.53564647G>A	GRCh37
NC_000023.9:g.53581372G>A	NCBI36
NG_016261.2:g.154048C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704099.1:c.11791C>T	ENSP00000515693.1:p.Gln3931Ter
ENST00000262854.11:c.12007C>T MANE Select	ENSP00000262854.6:p.Gln4003Ter
ENST00000262854.10:c.12007C>T	ENSP00000262854.6:p.Gln4003Ter
ENST00000342160.7:c.12007C>T	ENSP00000340648.3:p.Gln4003Ter
ENST00000426907.5:c.2474C>T
ENST00000480438.1:n.142C>T
ENST00000612484.4:c.11980C>T	ENSP00000479451.1:p.Gln3994Ter
NM_031407.6:c.12007C>T	NP_113584.3:p.Gln4003Ter
XM_005261965.2:c.12007C>T	XP_005262022.1:p.Gln4003Ter
XM_011530746.1:c.12256C>T	XP_011529048.1:p.Gln4086Ter
XM_011530747.1:c.12256C>T	XP_011529049.1:p.Gln4086Ter
XM_011530748.1:c.12256C>T	XP_011529050.1:p.Gln4086Ter
XM_011530749.1:c.12256C>T	XP_011529051.1:p.Gln4086Ter
XM_011530750.1:c.12256C>T	XP_011529052.1:p.Gln4086Ter
XM_011530751.1:c.12256C>T	XP_011529053.1:p.Gln4086Ter
XM_011530752.1:c.12253C>T	XP_011529054.1:p.Gln4085Ter
XM_011530753.1:c.12211C>T	XP_011529055.1:p.Gln4071Ter
XM_011530754.1:c.12208C>T	XP_011529056.1:p.Gln4070Ter
XM_011530755.1:c.12205C>T	XP_011529057.1:p.Gln4069Ter
XM_011530756.1:c.12157C>T	XP_011529058.1:p.Gln4053Ter
XM_011530757.1:c.11854C>T	XP_011529059.1:p.Gln3952Ter
XM_005261965.4:c.12007C>T	XP_005262022.1:p.Gln4003Ter
XM_011530751.2:c.12256C>T	XP_011529053.1:p.Gln4086Ter
XM_017029191.1:c.12388C>T	XP_016884680.1:p.Gln4130Ter
XM_017029192.1:c.12385C>T	XP_016884681.1:p.Gln4129Ter
XM_017029193.1:c.12367C>T	XP_016884682.1:p.Gln4123Ter
XM_017029194.1:c.12343C>T	XP_016884683.1:p.Gln4115Ter
XM_017029195.1:c.12340C>T	XP_016884684.1:p.Gln4114Ter
XM_017029196.1:c.12337C>T	XP_016884685.1:p.Gln4113Ter
XM_017029197.1:c.12289C>T	XP_016884686.1:p.Gln4097Ter
XM_017029198.2:c.12277C>T	XP_016884687.1:p.Gln4093Ter
XM_017029199.1:c.12277C>T	XP_016884688.1:p.Gln4093Ter
XM_017029200.1:c.12277C>T	XP_016884689.1:p.Gln4093Ter
XM_017029201.1:c.12277C>T	XP_016884690.1:p.Gln4093Ter
XM_017029202.1:c.12277C>T	XP_016884691.1:p.Gln4093Ter
XM_017029203.1:c.12277C>T	XP_016884692.1:p.Gln4093Ter
XM_017029204.1:c.12139C>T	XP_016884693.1:p.Gln4047Ter
XM_017029206.1:c.11986C>T	XP_016884695.1:p.Gln3996Ter
XM_024452322.1:c.12256C>T	XP_024308090.1:p.Gln4086Ter
NM_031407.7:c.12007C>T MANE Select	NP_113584.3:p.Gln4003Ter