Canonical Allele Identifier: CA250335

Gene: TRNT1 CRBN

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.3151023A>G , CM000665.2:g.3151023A>G	GRCh38
NC_000003.11:g.3192707A>G , CM000665.1:g.3192707A>G	GRCh37
NC_000003.10:g.3167707A>G	NCBI36
NG_016864.1:g.33695T>C
NG_041800.1:g.29108A>G
NG_041800.2:g.29108A>G
NG_016864.2:g.33695T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_016302.4:c.1171T>C (CRBN) MANE Select	NP_057386.2:p.Cys391Arg
ENST00000231948.9:c.1171T>C (CRBN) MANE Select	ENSP00000231948.4:p.Cys391Arg
NM_001173482.1:c.1168T>C (CRBN)	NP_001166953.1:p.Cys390Arg
NM_001367321.1:c.*517A>G (TRNT1)	NP_001354250.1:n.*517A>G
NM_016302.3:c.1171T>C (CRBN)	NP_057386.2:p.Cys391Arg
NR_159934.1:n.2040A>G (TRNT1)
NR_159935.1:n.1557-1391A>G (TRNT1)
NR_159936.1:n.1846A>G (TRNT1)
NR_159937.1:n.3082A>G (TRNT1)
ENST00000231948.8:c.1171T>C (CRBN)	ENSP00000231948.4:p.Cys391Arg
ENST00000424814.5:c.1026T>C (CRBN)
ENST00000432408.6:c.1168T>C (CRBN)	ENSP00000412499.2:p.Cys390Arg
ENST00000459840.5:n.560T>C (CRBN)
ENST00000488263.5:n.3516T>C (CRBN)
ENST00000491834.5:n.3597T>C (CRBN)
ENST00000498442.1:n.453T>C (CRBN)
ENST00000639284.1:c.1171T>C (CRBN)	ENSP00000491442.1:p.Cys391Arg
ENST00000698406.1:c.*34-1391A>G (TRNT1)	ENSP00000513700.1:n.*34-1391A>G
ENST00000698407.1:n.4803A>G (TRNT1)
ENST00000698408.1:c.*174-1391A>G (TRNT1)	ENSP00000513701.1:n.*174-1391A>G
ENST00000698410.1:c.*3645A>G (TRNT1)	ENSP00000513703.1:n.*3645A>G
ENST00000698412.1:c.*2869A>G (TRNT1)	ENSP00000513705.1:n.*2869A>G
ENST00000698413.1:c.*2869A>G (TRNT1)	ENSP00000513706.1:n.*2869A>G
ENST00000698414.1:c.*2869A>G (TRNT1)	ENSP00000513707.1:n.*2869A>G
ENST00000698415.1:n.5535A>G (TRNT1)
ENST00000698416.1:n.4438A>G (TRNT1)
XM_005265202.2:c.982T>C (CRBN)	XP_005265259.1:p.Cys328Arg
XM_005265202.4:c.982T>C (CRBN)	XP_005265259.1:p.Cys328Arg
XM_011533778.3:c.*517A>G (TRNT1)	XP_011532080.1:n.*517A>G
XM_011533791.1:c.1039T>C (CRBN)	XP_011532093.1:p.Cys347Arg
XM_011533791.3:c.1039T>C (CRBN)	XP_011532093.1:p.Cys347Arg
XM_011533792.1:c.*68T>C (CRBN)	XP_011532094.1:n.*68T>C
XM_011533793.1:c.679T>C (CRBN)	XP_011532095.1:p.Cys227Arg
XM_011533793.2:c.679T>C (CRBN)	XP_011532095.1:p.Cys227Arg
XM_011533794.1:c.679T>C (CRBN)	XP_011532096.1:p.Cys227Arg
XM_011533794.2:c.679T>C (CRBN)	XP_011532096.1:p.Cys227Arg
XM_024453551.1:c.*68T>C (CRBN)	XP_024309319.1:n.*68T>C
XR_001740169.2:n.2466-1391A>G (TRNT1)
XR_940445.3:n.2043A>G (TRNT1)
XR_940446.1:n.1581-1391A>G (TRNT1)
XR_940446.3:n.1560-1391A>G (TRNT1)
XR_940448.1:n.1072T>C (CRBN)
XR_940448.3:n.1069T>C (CRBN)