Canonical Allele Identifier: CA351453081

Gene: CRBN

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.3172870G>A , CM000665.2:g.3172870G>A	GRCh38
NC_000003.11:g.3214554G>A , CM000665.1:g.3214554G>A	GRCh37
NC_000003.10:g.3189554G>A	NCBI36
NG_016864.1:g.11848C>T
NG_016864.2:g.11848C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_016302.4:c.433C>T MANE Select	NP_057386.2:p.Arg145Ter
ENST00000231948.9:c.433C>T MANE Select	ENSP00000231948.4:p.Arg145Ter
NM_001173482.1:c.430C>T	NP_001166953.1:p.Arg144Ter
NM_016302.3:c.433C>T	NP_057386.2:p.Arg145Ter
ENST00000231948.8:c.433C>T	ENSP00000231948.4:p.Arg145Ter
ENST00000424814.5:c.420C>T
ENST00000432408.6:c.430C>T	ENSP00000412499.2:p.Arg144Ter
ENST00000450014.1:c.420C>T
ENST00000480249.5:n.119C>T
ENST00000482844.5:n.54C>T
ENST00000491834.5:n.330C>T
ENST00000492178.1:n.347C>T
ENST00000498700.5:n.447C>T
ENST00000639284.1:c.433C>T	ENSP00000491442.1:p.Arg145Ter
XM_005265202.2:c.244C>T	XP_005265259.1:p.Arg82Ter
XM_005265202.4:c.244C>T	XP_005265259.1:p.Arg82Ter
XM_011533791.1:c.433C>T	XP_011532093.1:p.Arg145Ter
XM_011533791.3:c.433C>T	XP_011532093.1:p.Arg145Ter
XM_011533792.1:c.433C>T	XP_011532094.1:p.Arg145Ter
XM_011533793.1:c.-201C>T	XP_011532095.1:n.-201C>T
XM_011533793.2:c.-201C>T	XP_011532095.1:n.-201C>T
XM_011533794.1:c.-201C>T	XP_011532096.1:n.-201C>T
XM_011533794.2:c.-201C>T	XP_011532096.1:n.-201C>T
XM_024453551.1:c.433C>T	XP_024309319.1:p.Arg145Ter
XR_940448.1:n.450C>T
XR_940448.3:n.447C>T