Canonical Allele Identifier: CA1044448476

Gene: CRBN

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.3157951A>T , CM000665.2:g.3157951A>T	GRCh38
NC_000003.11:g.3199635A>T , CM000665.1:g.3199635A>T	GRCh37
NC_000003.10:g.3174635A>T	NCBI36
NG_016864.1:g.26767T>A
NG_016864.2:g.26767T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231948.9:c.688-1670T>A MANE Select	ENSP00000231948.4:n.688-1670T>A
ENST00000639284.1:c.688-1670T>A	ENSP00000491442.1:n.688-1670T>A
ENST00000231948.8:c.688-1670T>A	ENSP00000231948.4:n.688-1670T>A
ENST00000424814.5:c.675-1670T>A
ENST00000432408.6:c.685-1670T>A	ENSP00000412499.2:n.685-1670T>A
ENST00000480249.5:n.374-1670T>A
ENST00000482844.5:n.309-1670T>A
ENST00000491834.5:n.585-1670T>A
NM_001173482.1:c.685-1670T>A	NP_001166953.1:n.685-1670T>A
NM_016302.3:c.688-1670T>A	NP_057386.2:n.688-1670T>A
XM_005265202.2:c.499-1670T>A	XP_005265259.1:n.499-1670T>A
XM_011533791.1:c.688-1670T>A	XP_011532093.1:n.688-1670T>A
XM_011533792.1:c.688-1670T>A	XP_011532094.1:n.688-1670T>A
XM_011533793.1:c.196-1670T>A	XP_011532095.1:n.196-1670T>A
XM_011533794.1:c.196-1670T>A	XP_011532096.1:n.196-1670T>A
XR_940448.1:n.705-1670T>A
XM_005265202.4:c.499-1670T>A	XP_005265259.1:n.499-1670T>A
XM_011533791.3:c.688-1670T>A	XP_011532093.1:n.688-1670T>A
XM_011533793.2:c.196-1670T>A	XP_011532095.1:n.196-1670T>A
XM_011533794.2:c.196-1670T>A	XP_011532096.1:n.196-1670T>A
XM_024453551.1:c.688-1670T>A	XP_024309319.1:n.688-1670T>A
XR_940448.3:n.702-1670T>A
NM_016302.4:c.688-1670T>A MANE Select	NP_057386.2:n.688-1670T>A