Canonical Allele Identifier: CA10505644

Gene: CUL4B

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.120547123T>C , CM000685.2:g.120547123T>C	GRCh38
NC_000023.10:g.119680978T>C , CM000685.1:g.119680978T>C	GRCh37
NC_000023.9:g.119565006T>C	NCBI36
NG_009388.1:g.33707A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001079872.2:c.776+13A>G MANE Select	NP_001073341.1:n.776+13A>G
ENST00000371322.11:c.776+13A>G MANE Select	ENSP00000360373.5:n.776+13A>G
NM_001079872.1:c.776+13A>G	NP_001073341.1:n.776+13A>G
NM_001330624.1:c.791+13A>G	NP_001317553.1:n.791+13A>G
NM_001330624.2:c.791+13A>G	NP_001317553.1:n.791+13A>G
NM_001369145.1:c.242+13A>G	NP_001356074.1:n.242+13A>G
NM_003588.3:c.830+13A>G	NP_003579.3:n.830+13A>G
NM_003588.4:c.830+13A>G	NP_003579.3:n.830+13A>G
ENST00000336592.10:c.791+13A>G	ENSP00000338919.6:n.791+13A>G
ENST00000336592.11:c.791+13A>G	ENSP00000338919.6:n.791+13A>G
ENST00000371322.9:c.776+13A>G	ENSP00000360373.5:n.776+13A>G
ENST00000371323.2:c.242+13A>G	ENSP00000360374.2:n.242+13A>G
ENST00000371323.3:c.242+13A>G	ENSP00000360374.3:n.242+13A>G
ENST00000404115.7:c.830+13A>G	ENSP00000384109.3:n.830+13A>G
ENST00000404115.8:c.776+13A>G	ENSP00000384109.4:n.776+13A>G
ENST00000673919.1:c.*223+13A>G	ENSP00000500994.1:n.*223+13A>G
ENST00000674073.2:c.220+13A>G
ENST00000674137.11:c.776+13A>G	ENSP00000501019.6:n.776+13A>G
ENST00000679405.1:c.360+13A>G	ENSP00000504985.1:n.360+13A>G
ENST00000679432.1:c.881+13A>G
ENST00000679844.1:c.220+13A>G
ENST00000679927.1:c.431+13A>G	ENSP00000505603.1:n.431+13A>G
ENST00000680165.1:n.1102+13A>G
ENST00000680324.1:n.690+13A>G
ENST00000680457.1:n.204+13A>G
ENST00000680474.1:c.220+13A>G
ENST00000680577.1:n.937+13A>G
ENST00000680673.1:c.830+13A>G	ENSP00000505084.1:n.830+13A>G
ENST00000680918.1:c.220+13A>G
ENST00000681080.1:c.266+13A>G
ENST00000681090.1:c.776+13A>G	ENSP00000506288.1:n.776+13A>G
ENST00000681189.1:c.220+13A>G
ENST00000681206.1:c.890+13A>G	ENSP00000505480.1:n.890+13A>G
ENST00000681253.1:c.830+13A>G	ENSP00000506259.1:n.830+13A>G
ENST00000681333.1:c.776+13A>G	ENSP00000505739.1:n.776+13A>G
ENST00000681652.1:c.830+13A>G	ENSP00000505176.1:n.830+13A>G
ENST00000681864.1:n.1420+13A>G
ENST00000681869.1:c.220+13A>G
ENST00000681908.1:c.220+13A>G
XM_005262481.1:c.830+13A>G	XP_005262538.1:n.830+13A>G
XM_006724784.1:c.791+13A>G	XP_006724847.1:n.791+13A>G
XM_006724785.1:c.791+13A>G	XP_006724848.1:n.791+13A>G
XM_011531399.1:c.242+13A>G	XP_011529701.1:n.242+13A>G
XM_011531399.2:c.242+13A>G	XP_011529701.1:n.242+13A>G
XM_011531400.1:c.242+13A>G	XP_011529702.1:n.242+13A>G
XM_011531400.2:c.242+13A>G	XP_011529702.1:n.242+13A>G
XM_011531401.1:c.188+13A>G	XP_011529703.1:n.188+13A>G