Canonical Allele Identifier: CA414205071

Gene: CUL4B

Linked Data

• MyVariant Identifiers: chrX:g.119694073T>C (hg19) ; chrX:g.120560218T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.120560218T>C , CM000685.2:g.120560218T>C	GRCh38
NC_000023.10:g.119694073T>C , CM000685.1:g.119694073T>C	GRCh37
NC_000023.9:g.119578101T>C	NCBI36
NG_009388.1:g.20612A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000336592.11:c.436A>G	ENSP00000338919.6:p.Asn146Asp
ENST00000371322.11:c.421A>G MANE Select	ENSP00000360373.5:p.Asn141Asp
ENST00000404115.8:c.421A>G	ENSP00000384109.4:p.Asn141Asp
ENST00000467641.2:n.88A>G
ENST00000673919.1:c.421A>G	ENSP00000500994.1:p.Asn141Asp
ENST00000674137.11:c.421A>G	ENSP00000501019.6:p.Asn141Asp
ENST00000679432.1:c.408A>G
ENST00000679927.1:c.76A>G	ENSP00000505603.1:p.Asn26Asp
ENST00000680165.1:n.747A>G
ENST00000680324.1:n.335A>G
ENST00000680577.1:n.582A>G
ENST00000680673.1:c.475A>G	ENSP00000505084.1:p.Asn159Asp
ENST00000681090.1:c.421A>G	ENSP00000506288.1:p.Asn141Asp
ENST00000681206.1:c.436A>G	ENSP00000505480.1:p.Asn146Asp
ENST00000681253.1:c.475A>G	ENSP00000506259.1:p.Asn159Asp
ENST00000681333.1:c.421A>G	ENSP00000505739.1:p.Asn141Asp
ENST00000681652.1:c.475A>G	ENSP00000505176.1:p.Asn159Asp
ENST00000336592.10:c.436A>G	ENSP00000338919.6:p.Asn146Asp
ENST00000371322.9:c.421A>G	ENSP00000360373.5:p.Asn141Asp
ENST00000404115.7:c.475A>G	ENSP00000384109.3:p.Asn159Asp
ENST00000467641.1:n.578A>G
NM_001079872.1:c.421A>G	NP_001073341.1:p.Asn141Asp
NM_003588.3:c.475A>G	NP_003579.3:p.Asn159Asp
XM_005262481.1:c.475A>G	XP_005262538.1:p.Asn159Asp
XM_006724784.1:c.436A>G	XP_006724847.1:p.Asn146Asp
XM_006724785.1:c.436A>G	XP_006724848.1:p.Asn146Asp
NM_001330624.1:c.436A>G	NP_001317553.1:p.Asn146Asp
NM_001079872.2:c.421A>G MANE Select	NP_001073341.1:p.Asn141Asp
NM_001330624.2:c.436A>G	NP_001317553.1:p.Asn146Asp
NM_003588.4:c.475A>G	NP_003579.3:p.Asn159Asp