Canonical Allele Identifier: CA2229040

Gene: TRNT1 CRBN

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.3152447T>C , CM000665.2:g.3152447T>C	GRCh38
NC_000003.11:g.3194131T>C , CM000665.1:g.3194131T>C	GRCh37
NC_000003.10:g.3169131T>C	NCBI36
NG_016864.1:g.32271A>G
NG_041800.2:g.30532T>C
NG_016864.2:g.32271A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_016302.4:c.1148+9A>G (CRBN) MANE Select	NP_057386.2:n.1148+9A>G
ENST00000231948.9:c.1148+9A>G (CRBN) MANE Select	ENSP00000231948.4:n.1148+9A>G
NM_001173482.1:c.1145+9A>G (CRBN)	NP_001166953.1:n.1145+9A>G
NM_001367321.1:c.*1941T>C (TRNT1)	NP_001354250.1:n.*1941T>C
NM_016302.3:c.1148+9A>G (CRBN)	NP_057386.2:n.1148+9A>G
NR_159934.1:n.3464T>C (TRNT1)
NR_159935.1:n.1590T>C (TRNT1)
NR_159936.1:n.3270T>C (TRNT1)
NR_159937.1:n.4506T>C (TRNT1)
ENST00000231948.8:c.1148+9A>G (CRBN)	ENSP00000231948.4:n.1148+9A>G
ENST00000424814.5:c.1003+977A>G (CRBN)
ENST00000432408.6:c.1145+9A>G (CRBN)	ENSP00000412499.2:n.1145+9A>G
ENST00000459840.5:n.537+9A>G (CRBN)
ENST00000488263.5:n.3493+9A>G (CRBN)
ENST00000491834.5:n.3574+9A>G (CRBN)
ENST00000498442.1:n.430+9A>G (CRBN)
ENST00000639284.1:c.1148+9A>G (CRBN)	ENSP00000491442.1:n.1148+9A>G
ENST00000698406.1:c.*67T>C (TRNT1)	ENSP00000513700.1:n.*67T>C
ENST00000698408.1:c.*207T>C (TRNT1)	ENSP00000513701.1:n.*207T>C
ENST00000698410.1:c.*5069T>C (TRNT1)	ENSP00000513703.1:n.*5069T>C
ENST00000698412.1:c.*4293T>C (TRNT1)	ENSP00000513705.1:n.*4293T>C
XM_005265202.2:c.959+9A>G (CRBN)	XP_005265259.1:n.959+9A>G
XM_005265202.4:c.959+9A>G (CRBN)	XP_005265259.1:n.959+9A>G
XM_011533778.3:c.*1941T>C (TRNT1)	XP_011532080.1:n.*1941T>C
XM_011533791.1:c.1016+977A>G (CRBN)	XP_011532093.1:n.1016+977A>G
XM_011533791.3:c.1016+977A>G (CRBN)	XP_011532093.1:n.1016+977A>G
XM_011533792.1:c.*45+977A>G (CRBN)	XP_011532094.1:n.*45+977A>G
XM_011533793.1:c.656+9A>G (CRBN)	XP_011532095.1:n.656+9A>G
XM_011533793.2:c.656+9A>G (CRBN)	XP_011532095.1:n.656+9A>G
XM_011533794.1:c.656+9A>G (CRBN)	XP_011532096.1:n.656+9A>G
XM_011533794.2:c.656+9A>G (CRBN)	XP_011532096.1:n.656+9A>G
XM_024453551.1:c.*45+977A>G (CRBN)	XP_024309319.1:n.*45+977A>G
XR_001740169.2:n.2499T>C (TRNT1)
XR_940445.3:n.3467T>C (TRNT1)
XR_940446.1:n.1614T>C (TRNT1)
XR_940446.3:n.1593T>C (TRNT1)
XR_940448.1:n.1049+9A>G (CRBN)
XR_940448.3:n.1046+9A>G (CRBN)