Canonical Allele Identifier: CA334126022

Gene: CUL4B

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.120546610T>C , CM000685.2:g.120546610T>C	GRCh38
NC_000023.10:g.119680465T>C , CM000685.1:g.119680465T>C	GRCh37
NC_000023.9:g.119564493T>C	NCBI36
NG_009388.1:g.34220A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001079872.2:c.783A>G MANE Select	NP_001073341.1:p.Ser261=
ENST00000371322.11:c.783A>G MANE Select	ENSP00000360373.5:p.Ser261=
NM_001079872.1:c.783A>G	NP_001073341.1:p.Ser261=
NM_001330624.1:c.798A>G	NP_001317553.1:p.Ser266=
NM_001330624.2:c.798A>G	NP_001317553.1:p.Ser266=
NM_001369145.1:c.249A>G	NP_001356074.1:p.Ser83=
NM_003588.3:c.837A>G	NP_003579.3:p.Ser279=
NM_003588.4:c.837A>G	NP_003579.3:p.Ser279=
ENST00000336592.10:c.798A>G	ENSP00000338919.6:p.Ser266=
ENST00000336592.11:c.798A>G	ENSP00000338919.6:p.Ser266=
ENST00000371322.9:c.783A>G	ENSP00000360373.5:p.Ser261=
ENST00000371323.2:c.249A>G	ENSP00000360374.2:p.Ser83=
ENST00000371323.3:c.249A>G	ENSP00000360374.3:p.Ser83=
ENST00000404115.7:c.837A>G	ENSP00000384109.3:p.Ser279=
ENST00000404115.8:c.783A>G	ENSP00000384109.4:p.Ser261=
ENST00000673919.1:c.*230A>G	ENSP00000500994.1:n.*230A>G
ENST00000674073.2:c.227A>G
ENST00000674137.11:c.783A>G	ENSP00000501019.6:p.Ser261=
ENST00000679405.1:c.367A>G	ENSP00000504985.1:p.Ile123Val
ENST00000679432.1:c.888A>G
ENST00000679844.1:c.227A>G
ENST00000679927.1:c.438A>G	ENSP00000505603.1:p.Ser146=
ENST00000680165.1:n.1109A>G
ENST00000680324.1:n.697A>G
ENST00000680457.1:n.211A>G
ENST00000680474.1:c.227A>G
ENST00000680577.1:n.944A>G
ENST00000680673.1:c.837A>G	ENSP00000505084.1:p.Ser279=
ENST00000680918.1:c.227A>G
ENST00000681080.1:c.273A>G
ENST00000681090.1:c.783A>G	ENSP00000506288.1:p.Ser261=
ENST00000681189.1:c.227A>G
ENST00000681206.1:c.897A>G	ENSP00000505480.1:p.Ser299=
ENST00000681224.1:n.63A>G
ENST00000681253.1:c.837A>G	ENSP00000506259.1:p.Ser279=
ENST00000681333.1:c.783A>G	ENSP00000505739.1:p.Ser261=
ENST00000681652.1:c.837A>G	ENSP00000505176.1:p.Ser279=
ENST00000681864.1:n.1427A>G
ENST00000681869.1:c.227A>G
ENST00000681908.1:c.227A>G
XM_005262481.1:c.837A>G	XP_005262538.1:p.Ser279=
XM_006724784.1:c.798A>G	XP_006724847.1:p.Ser266=
XM_006724785.1:c.798A>G	XP_006724848.1:p.Ser266=
XM_011531399.1:c.249A>G	XP_011529701.1:p.Ser83=
XM_011531399.2:c.249A>G	XP_011529701.1:p.Ser83=
XM_011531400.1:c.249A>G	XP_011529702.1:p.Ser83=
XM_011531400.2:c.249A>G	XP_011529702.1:p.Ser83=
XM_011531401.1:c.195A>G	XP_011529703.1:p.Ser65=