Canonical Allele Identifier: CA351452614

Gene: CRBN

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.3167680G>C , CM000665.2:g.3167680G>C	GRCh38
NC_000003.11:g.3209364G>C , CM000665.1:g.3209364G>C	GRCh37
NC_000003.10:g.3184364G>C	NCBI36
NG_016864.1:g.17038C>G
NG_016864.2:g.17038C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231948.9:c.641C>G MANE Select	ENSP00000231948.4:p.Ser214Ter
ENST00000639284.1:c.641C>G	ENSP00000491442.1:p.Ser214Ter
ENST00000231948.8:c.641C>G	ENSP00000231948.4:p.Ser214Ter
ENST00000424814.5:c.628C>G
ENST00000432408.6:c.638C>G	ENSP00000412499.2:p.Ser213Ter
ENST00000450014.1:c.628C>G
ENST00000480249.5:n.327C>G
ENST00000482844.5:n.262C>G
ENST00000491834.5:n.538C>G
NM_001173482.1:c.638C>G	NP_001166953.1:p.Ser213Ter
NM_016302.3:c.641C>G	NP_057386.2:p.Ser214Ter
XM_005265202.2:c.452C>G	XP_005265259.1:p.Ser151Ter
XM_011533791.1:c.641C>G	XP_011532093.1:p.Ser214Ter
XM_011533792.1:c.641C>G	XP_011532094.1:p.Ser214Ter
XM_011533793.1:c.149C>G	XP_011532095.1:p.Ser50Ter
XM_011533794.1:c.149C>G	XP_011532096.1:p.Ser50Ter
XR_940448.1:n.658C>G
XM_005265202.4:c.452C>G	XP_005265259.1:p.Ser151Ter
XM_011533791.3:c.641C>G	XP_011532093.1:p.Ser214Ter
XM_011533793.2:c.149C>G	XP_011532095.1:p.Ser50Ter
XM_011533794.2:c.149C>G	XP_011532096.1:p.Ser50Ter
XM_024453551.1:c.641C>G	XP_024309319.1:p.Ser214Ter
XR_940448.3:n.655C>G
NM_016302.4:c.641C>G MANE Select	NP_057386.2:p.Ser214Ter