Canonical Allele Identifier: CA2229431
Gene: CRBN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.3179661G>C , CM000665.2:g.3179661G>C GRCh38
NC_000003.11:g.3221345G>C , CM000665.1:g.3221345G>C GRCh37
NC_000003.10:g.3196345G>C NCBI36
NG_016864.1:g.5057C>G
NG_016864.2:g.5057C>G

Transcript Alleles

HGVS Amino-acid Change
NM_016302.4:c.27C>G MANE Select NP_057386.2:p.Asp9Glu
ENST00000231948.9:c.27C>G MANE Select ENSP00000231948.4:p.Asp9Glu
NM_001173482.1:c.27C>G NP_001166953.1:p.Asp9Glu
NM_016302.3:c.27C>G NP_057386.2:p.Asp9Glu
ENST00000231948.8:c.27C>G ENSP00000231948.4:p.Asp9Glu
ENST00000424814.5:c.14C>G
ENST00000432408.6:c.27C>G ENSP00000412499.2:p.Asp9Glu
ENST00000450014.1:c.14C>G
ENST00000478353.1:n.44C>G
ENST00000491834.5:n.31C>G
ENST00000498700.5:n.41C>G
ENST00000639284.1:c.27C>G ENSP00000491442.1:p.Asp9Glu
XM_005265202.2:c.-56C>G XP_005265259.1:n.-56C>G
XM_005265202.4:c.-56C>G XP_005265259.1:n.-56C>G
XM_011533791.1:c.27C>G XP_011532093.1:p.Asp9Glu
XM_011533791.3:c.27C>G XP_011532093.1:p.Asp9Glu
XM_011533792.1:c.27C>G XP_011532094.1:p.Asp9Glu
XM_011533793.1:c.-607C>G XP_011532095.1:n.-607C>G
XM_011533793.2:c.-607C>G XP_011532095.1:n.-607C>G
XM_011533794.1:c.-500C>G XP_011532096.1:n.-500C>G
XM_011533794.2:c.-500C>G XP_011532096.1:n.-500C>G
XM_024453551.1:c.27C>G XP_024309319.1:p.Asp9Glu
XR_940448.1:n.44C>G
XR_940448.3:n.41C>G