Canonical Allele Identifier: CA414204732

Gene: CUL4B

Linked Data

• MyVariant Identifiers: chrX:g.119693977G>T (hg19) ; chrX:g.120560122G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.120560122G>T , CM000685.2:g.120560122G>T	GRCh38
NC_000023.10:g.119693977G>T , CM000685.1:g.119693977G>T	GRCh37
NC_000023.9:g.119578005G>T	NCBI36
NG_009388.1:g.20708C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000336592.11:c.532C>A	ENSP00000338919.6:p.Pro178Thr
ENST00000371322.11:c.517C>A MANE Select	ENSP00000360373.5:p.Pro173Thr
ENST00000404115.8:c.517C>A	ENSP00000384109.4:p.Pro173Thr
ENST00000467641.2:n.184C>A
ENST00000673919.1:c.517C>A	ENSP00000500994.1:p.Pro173Thr
ENST00000674137.11:c.517C>A	ENSP00000501019.6:p.Pro173Thr
ENST00000679432.1:c.504C>A
ENST00000679927.1:c.172C>A	ENSP00000505603.1:p.Pro58Thr
ENST00000680165.1:n.843C>A
ENST00000680324.1:n.431C>A
ENST00000680577.1:n.678C>A
ENST00000680673.1:c.571C>A	ENSP00000505084.1:p.Pro191Thr
ENST00000681090.1:c.517C>A	ENSP00000506288.1:p.Pro173Thr
ENST00000681206.1:c.532C>A	ENSP00000505480.1:p.Pro178Thr
ENST00000681253.1:c.571C>A	ENSP00000506259.1:p.Pro191Thr
ENST00000681333.1:c.517C>A	ENSP00000505739.1:p.Pro173Thr
ENST00000681652.1:c.571C>A	ENSP00000505176.1:p.Pro191Thr
ENST00000336592.10:c.532C>A	ENSP00000338919.6:p.Pro178Thr
ENST00000371322.9:c.517C>A	ENSP00000360373.5:p.Pro173Thr
ENST00000404115.7:c.571C>A	ENSP00000384109.3:p.Pro191Thr
ENST00000467641.1:n.674C>A
NM_001079872.1:c.517C>A	NP_001073341.1:p.Pro173Thr
NM_003588.3:c.571C>A	NP_003579.3:p.Pro191Thr
XM_005262481.1:c.571C>A	XP_005262538.1:p.Pro191Thr
XM_006724784.1:c.532C>A	XP_006724847.1:p.Pro178Thr
XM_006724785.1:c.532C>A	XP_006724848.1:p.Pro178Thr
NM_001330624.1:c.532C>A	NP_001317553.1:p.Pro178Thr
NM_001079872.2:c.517C>A MANE Select	NP_001073341.1:p.Pro173Thr
NM_001330624.2:c.532C>A	NP_001317553.1:p.Pro178Thr
NM_003588.4:c.571C>A	NP_003579.3:p.Pro191Thr