Canonical Allele Identifier: CA645294134
Gene: CUL4B HGNC NCBI

Linked Data

ClinVar Variation Id: 426723
dbSNP Id: rs1085307760

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.120544610_120544614del , CM000685.2:g.120544610_120544614del GRCh38
NC_000023.10:g.119678465_119678469del , CM000685.1:g.119678465_119678469del GRCh37
NC_000023.9:g.119562493_119562497del NCBI36
NG_009388.1:g.36219_36223del

Transcript Alleles

HGVS Amino-acid change
ENST00000336592.11:c.968_972del ENSP00000338919.6:p.Ile323LysfsTer2
ENST00000371322.11:c.953_957del MANE Select ENSP00000360373.5:p.Ile318LysfsTer2
ENST00000371323.3:c.419_423del ENSP00000360374.3:p.Ile140LysfsTer2
ENST00000404115.8:c.953_957del ENSP00000384109.4:p.Ile318LysfsTer2
ENST00000673919.1:c.*400_*404del ENSP00000500994.1:n.*400_*404del
ENST00000674073.2:c.397_401del
ENST00000674137.11:c.953_957del ENSP00000501019.6:p.Ile318LysfsTer2
ENST00000679405.1:c.*162_*166del ENSP00000504985.1:n.*162_*166del
ENST00000679432.1:c.1058_1062del
ENST00000679844.1:c.397_401del
ENST00000679927.1:c.608_612del ENSP00000505603.1:p.Ile203LysfsTer2
ENST00000680165.1:n.1279_1283del
ENST00000680324.1:n.867_871del
ENST00000680457.1:n.381_385del
ENST00000680474.1:c.397_401del
ENST00000680577.1:n.1114_1118del
ENST00000680673.1:c.1007_1011del ENSP00000505084.1:p.Ile336LysfsTer2
ENST00000680918.1:c.365-408_365-404del
ENST00000681080.1:c.443_447del
ENST00000681090.1:c.921-61_921-57del ENSP00000506288.1:n.921-61_921-57del
ENST00000681189.1:c.397_401del
ENST00000681206.1:c.1067_1071del ENSP00000505480.1:p.Ile356LysfsTer2
ENST00000681224.1:n.233_237del
ENST00000681253.1:c.1007_1011del ENSP00000506259.1:p.Ile336LysfsTer2
ENST00000681333.1:c.953_957del ENSP00000505739.1:p.Ile318LysfsTer2
ENST00000681652.1:c.1007_1011del ENSP00000505176.1:p.Ile336LysfsTer2
ENST00000681864.1:n.1597_1601del
ENST00000681869.1:c.397_401del
ENST00000681908.1:c.397_401del
ENST00000336592.10:c.968_972del ENSP00000338919.6:p.Ile323LysfsTer2
ENST00000371322.9:c.953_957del ENSP00000360373.5:p.Ile318LysfsTer2
ENST00000371323.2:c.419_423del ENSP00000360374.2:p.Ile140LysfsTer2
ENST00000404115.7:c.1007_1011del ENSP00000384109.3:p.Ile336LysfsTer2
NM_001079872.1:c.953_957del NP_001073341.1:p.Ile318LysfsTer2
NM_003588.3:c.1007_1011del NP_003579.3:p.Ile336LysfsTer2
XM_005262481.1:c.1007_1011del XP_005262538.1:p.Ile336LysfsTer2
XM_006724784.1:c.968_972del XP_006724847.1:p.Ile323LysfsTer2
XM_006724785.1:c.968_972del XP_006724848.1:p.Ile323LysfsTer2
XM_011531399.1:c.419_423del XP_011529701.1:p.Ile140LysfsTer2
XM_011531400.1:c.419_423del XP_011529702.1:p.Ile140LysfsTer2
XM_011531401.1:c.365_369del XP_011529703.1:p.Ile122LysfsTer2
NM_001330624.1:c.968_972del NP_001317553.1:p.Ile323LysfsTer2
XM_011531399.2:c.419_423del XP_011529701.1:p.Ile140LysfsTer2
XM_011531400.2:c.419_423del XP_011529702.1:p.Ile140LysfsTer2
NM_001079872.2:c.953_957del MANE Select NP_001073341.1:p.Ile318LysfsTer2
NM_001369145.1:c.419_423del NP_001356074.1:p.Ile140LysfsTer2
NM_001330624.2:c.968_972del NP_001317553.1:p.Ile323LysfsTer2
NM_003588.4:c.1007_1011del NP_003579.3:p.Ile336LysfsTer2