Canonical Allele Identifier: CA206506

Gene: CRBN

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.3175249C>T , CM000665.2:g.3175249C>T	GRCh38
NC_000003.11:g.3216933C>T , CM000665.1:g.3216933C>T	GRCh37
NC_000003.10:g.3191933C>T	NCBI36
NG_016864.1:g.9469G>A
NG_016864.2:g.9469G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231948.9:c.88G>A MANE Select	ENSP00000231948.4:p.Glu30Lys
ENST00000639284.1:c.88G>A	ENSP00000491442.1:p.Glu30Lys
ENST00000231948.8:c.88G>A	ENSP00000231948.4:p.Glu30Lys
ENST00000424814.5:c.75G>A
ENST00000432408.6:c.85G>A	ENSP00000412499.2:p.Glu29Lys
ENST00000450014.1:c.75G>A
ENST00000478353.1:n.105G>A
ENST00000491834.5:n.72-988G>A
ENST00000492178.1:n.2G>A
ENST00000498700.5:n.102G>A
NM_001173482.1:c.85G>A	NP_001166953.1:p.Glu29Lys
NM_016302.3:c.88G>A	NP_057386.2:p.Glu30Lys
XM_005265202.2:c.-15-988G>A	XP_005265259.1:n.-15-988G>A
XM_011533791.1:c.88G>A	XP_011532093.1:p.Glu30Lys
XM_011533792.1:c.88G>A	XP_011532094.1:p.Glu30Lys
XM_011533793.1:c.-546G>A	XP_011532095.1:n.-546G>A
XM_011533794.1:c.-459-988G>A	XP_011532096.1:n.-459-988G>A
XR_940448.1:n.105G>A
XM_005265202.4:c.-15-988G>A	XP_005265259.1:n.-15-988G>A
XM_011533791.3:c.88G>A	XP_011532093.1:p.Glu30Lys
XM_011533793.2:c.-546G>A	XP_011532095.1:n.-546G>A
XM_011533794.2:c.-459-988G>A	XP_011532096.1:n.-459-988G>A
XM_024453551.1:c.88G>A	XP_024309319.1:p.Glu30Lys
XR_940448.3:n.102G>A
NM_016302.4:c.88G>A MANE Select	NP_057386.2:p.Glu30Lys