Canonical Allele Identifier: CA16043176
Gene: CUL4B HGNC NCBI

Linked Data

ClinVar Variation Id: 373768
ClinVar RCV Id: RCV000414203
dbSNP Id: rs1057518598

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.120526811_120526812del , CM000685.2:g.120526811_120526812del GRCh38
NC_000023.10:g.119660666_119660667del , CM000685.1:g.119660666_119660667del GRCh37
NC_000023.9:g.119544694_119544695del NCBI36
NG_009388.1:g.54018_54019del

Transcript Alleles

HGVS Amino-acid change
ENST00000336592.11:c.2652_2653del ENSP00000338919.6:p.Asp884GlufsTer6
ENST00000371322.11:c.2637_2638del MANE Select ENSP00000360373.5:p.Asp879GlufsTer6
ENST00000371323.3:c.2103_2104del ENSP00000360374.3:p.Asp701GlufsTer6
ENST00000404115.8:c.2484_2485del ENSP00000384109.4:p.Asp828GlufsTer6
ENST00000673919.1:c.*2084_*2085del ENSP00000500994.1:n.*2084_*2085del
ENST00000674073.2:c.1908_1909del
ENST00000674137.11:c.2643_2644del ENSP00000501019.6:p.Asp881GlufsTer6
ENST00000679405.1:c.*1846_*1847del ENSP00000504985.1:n.*1846_*1847del
ENST00000679432.1:c.2742_2743del
ENST00000679844.1:c.1976_1977del
ENST00000679927.1:c.2292_2293del ENSP00000505603.1:p.Asp764GlufsTer6
ENST00000679965.1:n.1217_1218del
ENST00000680165.1:n.3413_3414del
ENST00000680324.1:n.4045_4046del
ENST00000680457.1:n.2065_2066del
ENST00000680474.1:c.2143_2144del
ENST00000680577.1:n.3248_3249del
ENST00000680673.1:c.2691_2692del ENSP00000505084.1:p.Asp897GlufsTer6
ENST00000680918.1:c.1918_1919del
ENST00000681080.1:c.2127_2128del
ENST00000681090.1:c.2544_2545del ENSP00000506288.1:p.Asp848GlufsTer6
ENST00000681189.1:c.2143_2144del
ENST00000681206.1:c.2751_2752del ENSP00000505480.1:p.Asp917GlufsTer6
ENST00000681236.1:n.1241_1242del
ENST00000681253.1:c.2691_2692del ENSP00000506259.1:p.Asp897GlufsTer6
ENST00000681263.1:n.1481_1482del
ENST00000681333.1:c.*3530_*3531del ENSP00000505739.1:n.*3530_*3531del
ENST00000681487.1:n.1579_1580del
ENST00000681652.1:c.2691_2692del ENSP00000505176.1:p.Asp897GlufsTer6
ENST00000681706.1:n.668_669del
ENST00000681864.1:n.5225_5226del
ENST00000681908.1:c.2257_2258del
ENST00000336592.10:c.2652_2653del ENSP00000338919.6:p.Asp884GlufsTer6
ENST00000371322.9:c.2637_2638del ENSP00000360373.5:p.Asp879GlufsTer6
ENST00000404115.7:c.2691_2692del ENSP00000384109.3:p.Asp897GlufsTer6
NM_001079872.1:c.2637_2638del NP_001073341.1:p.Asp879GlufsTer6
NM_003588.3:c.2691_2692del NP_003579.3:p.Asp897GlufsTer6
XM_005262481.1:c.2697_2698del XP_005262538.1:p.Asp899GlufsTer6
XM_006724784.1:c.2658_2659del XP_006724847.1:p.Asp886GlufsTer6
XM_006724785.1:c.2652_2653del XP_006724848.1:p.Asp884GlufsTer6
XM_011531399.1:c.2109_2110del XP_011529701.1:p.Asp703GlufsTer6
XM_011531400.1:c.2103_2104del XP_011529702.1:p.Asp701GlufsTer6
XM_011531401.1:c.2055_2056del XP_011529703.1:p.Asp685GlufsTer6
NM_001330624.1:c.2652_2653del NP_001317553.1:p.Asp884GlufsTer6
XM_011531399.2:c.2109_2110del XP_011529701.1:p.Asp703GlufsTer6
XM_011531400.2:c.2103_2104del XP_011529702.1:p.Asp701GlufsTer6
NM_001079872.2:c.2637_2638del MANE Select NP_001073341.1:p.Asp879GlufsTer6
NM_001369145.1:c.2103_2104del NP_001356074.1:p.Asp701GlufsTer6
NM_001330624.2:c.2652_2653del NP_001317553.1:p.Asp884GlufsTer6
NM_003588.4:c.2691_2692del NP_003579.3:p.Asp897GlufsTer6