Canonical Allele Identifier: CA414192225

Gene: CUL4B

Linked Data

• ClinVar Variation Id: 434871
• ClinVar RCV Id: RCV000502107
• dbSNP Id: rs1556173896
• MyVariant Identifiers: chrX:g.119660671C>T (hg19) ; chrX:g.120526816C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.120526816C>T , CM000685.2:g.120526816C>T	GRCh38
NC_000023.10:g.119660671C>T , CM000685.1:g.119660671C>T	GRCh37
NC_000023.9:g.119544699C>T	NCBI36
NG_009388.1:g.54014G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336592.11:c.2648G>A	ENSP00000338919.6:p.Arg883Gln
ENST00000371322.11:c.2633G>A MANE Select	ENSP00000360373.5:p.Arg878Gln
ENST00000371323.3:c.2099G>A	ENSP00000360374.3:p.Arg700Gln
ENST00000404115.8:c.2480G>A	ENSP00000384109.4:p.Arg827Gln
ENST00000673919.1:c.*2080G>A	ENSP00000500994.1:n.*2080G>A
ENST00000674073.2:c.1904G>A
ENST00000674137.11:c.2639G>A	ENSP00000501019.6:p.Arg880Gln
ENST00000679405.1:c.*1842G>A	ENSP00000504985.1:n.*1842G>A
ENST00000679432.1:c.2738G>A
ENST00000679844.1:c.1972G>A
ENST00000679927.1:c.2288G>A	ENSP00000505603.1:p.Arg763Gln
ENST00000679965.1:n.1213G>A
ENST00000680165.1:n.3409G>A
ENST00000680324.1:n.4041G>A
ENST00000680457.1:n.2061G>A
ENST00000680474.1:c.2139G>A
ENST00000680577.1:n.3244G>A
ENST00000680673.1:c.2687G>A	ENSP00000505084.1:p.Arg896Gln
ENST00000680918.1:c.1914G>A
ENST00000681080.1:c.2123G>A
ENST00000681090.1:c.2540G>A	ENSP00000506288.1:p.Arg847Gln
ENST00000681189.1:c.2139G>A
ENST00000681206.1:c.2747G>A	ENSP00000505480.1:p.Arg916Gln
ENST00000681236.1:n.1237G>A
ENST00000681253.1:c.2687G>A	ENSP00000506259.1:p.Arg896Gln
ENST00000681263.1:n.1477G>A
ENST00000681333.1:c.*3526G>A	ENSP00000505739.1:n.*3526G>A
ENST00000681487.1:n.1575G>A
ENST00000681652.1:c.2687G>A	ENSP00000505176.1:p.Arg896Gln
ENST00000681706.1:n.664G>A
ENST00000681864.1:n.5221G>A
ENST00000681908.1:c.2253G>A
ENST00000336592.10:c.2648G>A	ENSP00000338919.6:p.Arg883Gln
ENST00000371322.9:c.2633G>A	ENSP00000360373.5:p.Arg878Gln
ENST00000404115.7:c.2687G>A	ENSP00000384109.3:p.Arg896Gln
NM_001079872.1:c.2633G>A	NP_001073341.1:p.Arg878Gln
NM_003588.3:c.2687G>A	NP_003579.3:p.Arg896Gln
XM_005262481.1:c.2693G>A	XP_005262538.1:p.Arg898Gln
XM_006724784.1:c.2654G>A	XP_006724847.1:p.Arg885Gln
XM_006724785.1:c.2648G>A	XP_006724848.1:p.Arg883Gln
XM_011531399.1:c.2105G>A	XP_011529701.1:p.Arg702Gln
XM_011531400.1:c.2099G>A	XP_011529702.1:p.Arg700Gln
XM_011531401.1:c.2051G>A	XP_011529703.1:p.Arg684Gln
NM_001330624.1:c.2648G>A	NP_001317553.1:p.Arg883Gln
XM_011531399.2:c.2105G>A	XP_011529701.1:p.Arg702Gln
XM_011531400.2:c.2099G>A	XP_011529702.1:p.Arg700Gln
NM_001079872.2:c.2633G>A MANE Select	NP_001073341.1:p.Arg878Gln
NM_001369145.1:c.2099G>A	NP_001356074.1:p.Arg700Gln
NM_001330624.2:c.2648G>A	NP_001317553.1:p.Arg883Gln
NM_003588.4:c.2687G>A	NP_003579.3:p.Arg896Gln