Canonical Allele Identifier: CA518448076

Gene: CUL4B

Linked Data

• MyVariant Identifiers: chrX:g.119694080T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.120560225T>C , CM000685.2:g.120560225T>C	GRCh38
NC_000023.10:g.119694080T>C , CM000685.1:g.119694080T>C	GRCh37
NC_000023.9:g.119578108T>C	NCBI36
NG_009388.1:g.20605A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000336592.11:c.429A>G	ENSP00000338919.6:p.Gln143=
ENST00000371322.11:c.414A>G MANE Select	ENSP00000360373.5:p.Gln138=
ENST00000404115.8:c.414A>G	ENSP00000384109.4:p.Gln138=
ENST00000467641.2:n.81A>G
ENST00000673919.1:c.414A>G	ENSP00000500994.1:p.Gln138=
ENST00000674137.11:c.414A>G	ENSP00000501019.6:p.Gln138=
ENST00000679432.1:c.401A>G
ENST00000679927.1:c.69A>G	ENSP00000505603.1:p.Gln23=
ENST00000680165.1:n.740A>G
ENST00000680324.1:n.328A>G
ENST00000680577.1:n.575A>G
ENST00000680673.1:c.468A>G	ENSP00000505084.1:p.Gln156=
ENST00000681090.1:c.414A>G	ENSP00000506288.1:p.Gln138=
ENST00000681206.1:c.429A>G	ENSP00000505480.1:p.Gln143=
ENST00000681253.1:c.468A>G	ENSP00000506259.1:p.Gln156=
ENST00000681333.1:c.414A>G	ENSP00000505739.1:p.Gln138=
ENST00000681652.1:c.468A>G	ENSP00000505176.1:p.Gln156=
ENST00000336592.10:c.429A>G	ENSP00000338919.6:p.Gln143=
ENST00000371322.9:c.414A>G	ENSP00000360373.5:p.Gln138=
ENST00000404115.7:c.468A>G	ENSP00000384109.3:p.Gln156=
ENST00000467641.1:n.571A>G
NM_001079872.1:c.414A>G	NP_001073341.1:p.Gln138=
NM_003588.3:c.468A>G	NP_003579.3:p.Gln156=
XM_005262481.1:c.468A>G	XP_005262538.1:p.Gln156=
XM_006724784.1:c.429A>G	XP_006724847.1:p.Gln143=
XM_006724785.1:c.429A>G	XP_006724848.1:p.Gln143=
NM_001330624.1:c.429A>G	NP_001317553.1:p.Gln143=
NM_001079872.2:c.414A>G MANE Select	NP_001073341.1:p.Gln138=
NM_001330624.2:c.429A>G	NP_001317553.1:p.Gln143=
NM_003588.4:c.468A>G	NP_003579.3:p.Gln156=