Canonical Allele Identifier: CA2229179

Gene: CRBN

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.3156245G>A , CM000665.2:g.3156245G>A	GRCh38
NC_000003.11:g.3197929G>A , CM000665.1:g.3197929G>A	GRCh37
NC_000003.10:g.3172929G>A	NCBI36
NG_016864.1:g.28473C>T
NG_016864.2:g.28473C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231948.9:c.724C>T MANE Select	ENSP00000231948.4:p.Arg242Cys
ENST00000639284.1:c.724C>T	ENSP00000491442.1:p.Arg242Cys
ENST00000231948.8:c.724C>T	ENSP00000231948.4:p.Arg242Cys
ENST00000424814.5:c.711C>T
ENST00000432408.6:c.721C>T	ENSP00000412499.2:p.Arg241Cys
ENST00000480249.5:n.410C>T
ENST00000482844.5:n.345C>T
ENST00000488263.5:n.540C>T
ENST00000491834.5:n.621C>T
NM_001173482.1:c.721C>T	NP_001166953.1:p.Arg241Cys
NM_016302.3:c.724C>T	NP_057386.2:p.Arg242Cys
XM_005265202.2:c.535C>T	XP_005265259.1:p.Arg179Cys
XM_011533791.1:c.724C>T	XP_011532093.1:p.Arg242Cys
XM_011533792.1:c.724C>T	XP_011532094.1:p.Arg242Cys
XM_011533793.1:c.232C>T	XP_011532095.1:p.Arg78Cys
XM_011533794.1:c.232C>T	XP_011532096.1:p.Arg78Cys
XR_940448.1:n.741C>T
XM_005265202.4:c.535C>T	XP_005265259.1:p.Arg179Cys
XM_011533791.3:c.724C>T	XP_011532093.1:p.Arg242Cys
XM_011533793.2:c.232C>T	XP_011532095.1:p.Arg78Cys
XM_011533794.2:c.232C>T	XP_011532096.1:p.Arg78Cys
XM_024453551.1:c.724C>T	XP_024309319.1:p.Arg242Cys
XR_940448.3:n.738C>T
NM_016302.4:c.724C>T MANE Select	NP_057386.2:p.Arg242Cys