Canonical Allele Identifier: CA10505491

Gene: CUL4B

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.120538715G>A , CM000685.2:g.120538715G>A	GRCh38
NC_000023.10:g.119672570G>A , CM000685.1:g.119672570G>A	GRCh37
NC_000023.9:g.119556598G>A	NCBI36
NG_009388.1:g.42115C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336592.11:c.1812C>T	ENSP00000338919.6:p.Val604=
ENST00000371322.11:c.1797C>T MANE Select	ENSP00000360373.5:p.Val599=
ENST00000371323.3:c.1263C>T	ENSP00000360374.3:p.Val421=
ENST00000404115.8:c.1797C>T	ENSP00000384109.4:p.Val599=
ENST00000673919.1:c.*1244C>T	ENSP00000500994.1:n.*1244C>T
ENST00000674073.2:c.1241C>T
ENST00000674137.11:c.1797C>T	ENSP00000501019.6:p.Val599=
ENST00000679405.1:c.*1006C>T	ENSP00000504985.1:n.*1006C>T
ENST00000679432.1:c.1902C>T
ENST00000679844.1:c.1136C>T
ENST00000679927.1:c.1452C>T	ENSP00000505603.1:p.Val484=
ENST00000679965.1:n.377C>T
ENST00000680165.1:n.2123C>T
ENST00000680324.1:n.3205C>T
ENST00000680457.1:n.1225C>T
ENST00000680474.1:c.1241C>T
ENST00000680577.1:n.1958C>T
ENST00000680673.1:c.1851C>T	ENSP00000505084.1:p.Val617=
ENST00000680918.1:c.1078C>T
ENST00000681080.1:c.1287C>T
ENST00000681090.1:c.1704C>T	ENSP00000506288.1:p.Val568=
ENST00000681189.1:c.1241C>T
ENST00000681206.1:c.1911C>T	ENSP00000505480.1:p.Val637=
ENST00000681253.1:c.1851C>T	ENSP00000506259.1:p.Val617=
ENST00000681263.1:n.191C>T
ENST00000681333.1:c.*2240C>T	ENSP00000505739.1:n.*2240C>T
ENST00000681652.1:c.1851C>T	ENSP00000505176.1:p.Val617=
ENST00000681864.1:n.3935C>T
ENST00000681869.1:c.1241C>T
ENST00000681908.1:c.1241C>T
ENST00000336592.10:c.1812C>T	ENSP00000338919.6:p.Val604=
ENST00000371322.9:c.1797C>T	ENSP00000360373.5:p.Val599=
ENST00000404115.7:c.1851C>T	ENSP00000384109.3:p.Val617=
NM_001079872.1:c.1797C>T	NP_001073341.1:p.Val599=
NM_003588.3:c.1851C>T	NP_003579.3:p.Val617=
XM_005262481.1:c.1851C>T	XP_005262538.1:p.Val617=
XM_006724784.1:c.1812C>T	XP_006724847.1:p.Val604=
XM_006724785.1:c.1812C>T	XP_006724848.1:p.Val604=
XM_011531399.1:c.1263C>T	XP_011529701.1:p.Val421=
XM_011531400.1:c.1263C>T	XP_011529702.1:p.Val421=
XM_011531401.1:c.1209C>T	XP_011529703.1:p.Val403=
NM_001330624.1:c.1812C>T	NP_001317553.1:p.Val604=
XM_011531399.2:c.1263C>T	XP_011529701.1:p.Val421=
XM_011531400.2:c.1263C>T	XP_011529702.1:p.Val421=
NM_001079872.2:c.1797C>T MANE Select	NP_001073341.1:p.Val599=
NM_001369145.1:c.1263C>T	NP_001356074.1:p.Val421=
NM_001330624.2:c.1812C>T	NP_001317553.1:p.Val604=
NM_003588.4:c.1851C>T	NP_003579.3:p.Val617=