Canonical Allele Identifier: CA10505670

Gene: CUL4B

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.120558023T>C , CM000685.2:g.120558023T>C	GRCh38
NC_000023.10:g.119691878T>C , CM000685.1:g.119691878T>C	GRCh37
NC_000023.9:g.119575906T>C	NCBI36
NG_009388.1:g.22807A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001079872.2:c.573A>G MANE Select	NP_001073341.1:p.Pro191=
ENST00000371322.11:c.573A>G MANE Select	ENSP00000360373.5:p.Pro191=
NM_001079872.1:c.573A>G	NP_001073341.1:p.Pro191=
NM_001330624.1:c.588A>G	NP_001317553.1:p.Pro196=
NM_001330624.2:c.588A>G	NP_001317553.1:p.Pro196=
NM_001369145.1:c.39A>G	NP_001356074.1:p.Pro13=
NM_003588.3:c.627A>G	NP_003579.3:p.Pro209=
NM_003588.4:c.627A>G	NP_003579.3:p.Pro209=
ENST00000336592.10:c.588A>G	ENSP00000338919.6:p.Pro196=
ENST00000336592.11:c.588A>G	ENSP00000338919.6:p.Pro196=
ENST00000371322.9:c.573A>G	ENSP00000360373.5:p.Pro191=
ENST00000371323.2:c.39A>G	ENSP00000360374.2:p.Pro13=
ENST00000371323.3:c.39A>G	ENSP00000360374.3:p.Pro13=
ENST00000404115.7:c.627A>G	ENSP00000384109.3:p.Pro209=
ENST00000404115.8:c.573A>G	ENSP00000384109.4:p.Pro191=
ENST00000467641.1:n.730A>G
ENST00000467641.2:n.240A>G
ENST00000673919.1:c.*20A>G	ENSP00000500994.1:n.*20A>G
ENST00000674073.2:c.17A>G
ENST00000674137.11:c.573A>G	ENSP00000501019.6:p.Pro191=
ENST00000679405.1:c.39A>G	ENSP00000504985.1:p.Pro13=
ENST00000679432.1:c.560A>G
ENST00000679844.1:c.17A>G
ENST00000679927.1:c.228A>G	ENSP00000505603.1:p.Pro76=
ENST00000680165.1:n.899A>G
ENST00000680324.1:n.487A>G
ENST00000680474.1:c.17A>G
ENST00000680577.1:n.734A>G
ENST00000680673.1:c.627A>G	ENSP00000505084.1:p.Pro209=
ENST00000680918.1:c.17A>G
ENST00000681080.1:c.17A>G
ENST00000681090.1:c.573A>G	ENSP00000506288.1:p.Pro191=
ENST00000681189.1:c.17A>G
ENST00000681206.1:c.588A>G	ENSP00000505480.1:p.Pro196=
ENST00000681253.1:c.627A>G	ENSP00000506259.1:p.Pro209=
ENST00000681333.1:c.573A>G	ENSP00000505739.1:p.Pro191=
ENST00000681652.1:c.627A>G	ENSP00000505176.1:p.Pro209=
ENST00000681869.1:c.17A>G
ENST00000681908.1:c.17A>G
XM_005262481.1:c.627A>G	XP_005262538.1:p.Pro209=
XM_006724784.1:c.588A>G	XP_006724847.1:p.Pro196=
XM_006724785.1:c.588A>G	XP_006724848.1:p.Pro196=
XM_011531399.1:c.39A>G	XP_011529701.1:p.Pro13=
XM_011531399.2:c.39A>G	XP_011529701.1:p.Pro13=
XM_011531400.1:c.39A>G	XP_011529702.1:p.Pro13=
XM_011531400.2:c.39A>G	XP_011529702.1:p.Pro13=