Canonical Allele Identifier: CA2229275

Gene: CRBN

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.3172865T>C , CM000665.2:g.3172865T>C	GRCh38
NC_000003.11:g.3214549T>C , CM000665.1:g.3214549T>C	GRCh37
NC_000003.10:g.3189549T>C	NCBI36
NG_016864.1:g.11853A>G
NG_016864.2:g.11853A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231948.9:c.438A>G MANE Select	ENSP00000231948.4:p.Glu146=
ENST00000639284.1:c.438A>G	ENSP00000491442.1:p.Glu146=
ENST00000231948.8:c.438A>G	ENSP00000231948.4:p.Glu146=
ENST00000424814.5:c.425A>G
ENST00000432408.6:c.435A>G	ENSP00000412499.2:p.Glu145=
ENST00000450014.1:c.425A>G
ENST00000480249.5:n.124A>G
ENST00000482844.5:n.59A>G
ENST00000491834.5:n.335A>G
ENST00000492178.1:n.352A>G
ENST00000498700.5:n.452A>G
NM_001173482.1:c.435A>G	NP_001166953.1:p.Glu145=
NM_016302.3:c.438A>G	NP_057386.2:p.Glu146=
XM_005265202.2:c.249A>G	XP_005265259.1:p.Glu83=
XM_011533791.1:c.438A>G	XP_011532093.1:p.Glu146=
XM_011533792.1:c.438A>G	XP_011532094.1:p.Glu146=
XM_011533793.1:c.-196A>G	XP_011532095.1:n.-196A>G
XM_011533794.1:c.-196A>G	XP_011532096.1:n.-196A>G
XR_940448.1:n.455A>G
XM_005265202.4:c.249A>G	XP_005265259.1:p.Glu83=
XM_011533791.3:c.438A>G	XP_011532093.1:p.Glu146=
XM_011533793.2:c.-196A>G	XP_011532095.1:n.-196A>G
XM_011533794.2:c.-196A>G	XP_011532096.1:n.-196A>G
XM_024453551.1:c.438A>G	XP_024309319.1:p.Glu146=
XR_940448.3:n.452A>G
NM_016302.4:c.438A>G MANE Select	NP_057386.2:p.Glu146=