Canonical Allele Identifier: CA2740092268

Gene: CUL4B

Linked Data

• ClinVar Variation Id: 3024245
• ClinVar RCV Id: RCV003883291

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.120560125del , CM000685.2:g.120560125del	GRCh38
NC_000023.10:g.119693980del , CM000685.1:g.119693980del	GRCh37
NC_000023.9:g.119578008del	NCBI36
NG_009388.1:g.20707del

Transcript Alleles

HGVS	Amino-acid change
ENST00000336592.11:c.531del	ENSP00000338919.6:p.Lys177AsnfsTer8
ENST00000371322.11:c.516del MANE Select	ENSP00000360373.5:p.Lys172AsnfsTer8
ENST00000404115.8:c.516del	ENSP00000384109.4:p.Lys172AsnfsTer8
ENST00000467641.2:n.183del
ENST00000673919.1:c.516del	ENSP00000500994.1:p.Lys172AsnfsTer8
ENST00000674137.11:c.516del	ENSP00000501019.6:p.Lys172AsnfsTer8
ENST00000679432.1:c.503del
ENST00000679927.1:c.171del	ENSP00000505603.1:p.Lys57AsnfsTer8
ENST00000680165.1:n.842del
ENST00000680324.1:n.430del
ENST00000680577.1:n.677del
ENST00000680673.1:c.570del	ENSP00000505084.1:p.Lys190AsnfsTer8
ENST00000681090.1:c.516del	ENSP00000506288.1:p.Lys172AsnfsTer8
ENST00000681206.1:c.531del	ENSP00000505480.1:p.Lys177AsnfsTer8
ENST00000681253.1:c.570del	ENSP00000506259.1:p.Lys190AsnfsTer8
ENST00000681333.1:c.516del	ENSP00000505739.1:p.Lys172AsnfsTer8
ENST00000681652.1:c.570del	ENSP00000505176.1:p.Lys190AsnfsTer8
ENST00000336592.10:c.531del	ENSP00000338919.6:p.Lys177AsnfsTer8
ENST00000371322.9:c.516del	ENSP00000360373.5:p.Lys172AsnfsTer8
ENST00000404115.7:c.570del	ENSP00000384109.3:p.Lys190AsnfsTer8
ENST00000467641.1:n.673del
NM_001079872.1:c.516del	NP_001073341.1:p.Lys172AsnfsTer8
NM_003588.3:c.570del	NP_003579.3:p.Lys190AsnfsTer8
XM_005262481.1:c.570del	XP_005262538.1:p.Lys190AsnfsTer8
XM_006724784.1:c.531del	XP_006724847.1:p.Lys177AsnfsTer8
XM_006724785.1:c.531del	XP_006724848.1:p.Lys177AsnfsTer8
NM_001330624.1:c.531del	NP_001317553.1:p.Lys177AsnfsTer8
NM_001079872.2:c.516del MANE Select	NP_001073341.1:p.Lys172AsnfsTer8
NM_001330624.2:c.531del	NP_001317553.1:p.Lys177AsnfsTer8
NM_003588.4:c.570del	NP_003579.3:p.Lys190AsnfsTer8