Canonical Allele Identifier: CA518448227

Gene: CUL4B

Linked Data

• MyVariant Identifiers: chrX:g.119694140C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.120560285C>T , CM000685.2:g.120560285C>T	GRCh38
NC_000023.10:g.119694140C>T , CM000685.1:g.119694140C>T	GRCh37
NC_000023.9:g.119578168C>T	NCBI36
NG_009388.1:g.20545G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336592.11:c.369G>A	ENSP00000338919.6:p.Glu123=
ENST00000371322.11:c.354G>A MANE Select	ENSP00000360373.5:p.Glu118=
ENST00000404115.8:c.354G>A	ENSP00000384109.4:p.Glu118=
ENST00000467641.2:n.21G>A
ENST00000673919.1:c.354G>A	ENSP00000500994.1:p.Glu118=
ENST00000674137.11:c.354G>A	ENSP00000501019.6:p.Glu118=
ENST00000679432.1:c.341G>A
ENST00000679927.1:c.9G>A	ENSP00000505603.1:p.Glu3=
ENST00000680165.1:n.680G>A
ENST00000680324.1:n.268G>A
ENST00000680577.1:n.515G>A
ENST00000680673.1:c.408G>A	ENSP00000505084.1:p.Glu136=
ENST00000681090.1:c.354G>A	ENSP00000506288.1:p.Glu118=
ENST00000681206.1:c.369G>A	ENSP00000505480.1:p.Glu123=
ENST00000681253.1:c.408G>A	ENSP00000506259.1:p.Glu136=
ENST00000681333.1:c.354G>A	ENSP00000505739.1:p.Glu118=
ENST00000681652.1:c.408G>A	ENSP00000505176.1:p.Glu136=
ENST00000336592.10:c.369G>A	ENSP00000338919.6:p.Glu123=
ENST00000371322.9:c.354G>A	ENSP00000360373.5:p.Glu118=
ENST00000404115.7:c.408G>A	ENSP00000384109.3:p.Glu136=
ENST00000467641.1:n.511G>A
NM_001079872.1:c.354G>A	NP_001073341.1:p.Glu118=
NM_003588.3:c.408G>A	NP_003579.3:p.Glu136=
XM_005262481.1:c.408G>A	XP_005262538.1:p.Glu136=
XM_006724784.1:c.369G>A	XP_006724847.1:p.Glu123=
XM_006724785.1:c.369G>A	XP_006724848.1:p.Glu123=
NM_001330624.1:c.369G>A	NP_001317553.1:p.Glu123=
NM_001079872.2:c.354G>A MANE Select	NP_001073341.1:p.Glu118=
NM_001330624.2:c.369G>A	NP_001317553.1:p.Glu123=
NM_003588.4:c.408G>A	NP_003579.3:p.Glu136=