Canonical Allele Identifier: CA351452121
Gene: CRBN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.3154791C>T , CM000665.2:g.3154791C>T GRCh38
NC_000003.11:g.3196475C>T , CM000665.1:g.3196475C>T GRCh37
NC_000003.10:g.3171475C>T NCBI36
NG_016864.1:g.29927G>A
NG_041800.2:g.32876C>T
NG_016864.2:g.29927G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000231948.9:c.791G>A MANE Select ENSP00000231948.4:p.Trp264Ter
ENST00000639284.1:c.791G>A ENSP00000491442.1:p.Trp264Ter
ENST00000231948.8:c.791G>A ENSP00000231948.4:p.Trp264Ter
ENST00000424814.5:c.778G>A
ENST00000432408.6:c.788G>A ENSP00000412499.2:p.Trp263Ter
ENST00000459840.5:n.180G>A
ENST00000482844.5:n.412G>A
ENST00000488263.5:n.1994G>A
ENST00000491834.5:n.2075G>A
NM_001173482.1:c.788G>A NP_001166953.1:p.Trp263Ter
NM_016302.3:c.791G>A NP_057386.2:p.Trp264Ter
XM_005265202.2:c.602G>A XP_005265259.1:p.Trp201Ter
XM_011533791.1:c.791G>A XP_011532093.1:p.Trp264Ter
XM_011533792.1:c.791G>A XP_011532094.1:p.Trp264Ter
XM_011533793.1:c.299G>A XP_011532095.1:p.Trp100Ter
XM_011533794.1:c.299G>A XP_011532096.1:p.Trp100Ter
XR_940448.1:n.808G>A
XM_005265202.4:c.602G>A XP_005265259.1:p.Trp201Ter
XM_011533791.3:c.791G>A XP_011532093.1:p.Trp264Ter
XM_011533793.2:c.299G>A XP_011532095.1:p.Trp100Ter
XM_011533794.2:c.299G>A XP_011532096.1:p.Trp100Ter
XM_024453551.1:c.791G>A XP_024309319.1:p.Trp264Ter
XR_940448.3:n.805G>A
NM_016302.4:c.791G>A MANE Select NP_057386.2:p.Trp264Ter