Canonical Allele Identifier: CA2228956

Gene: TRNT1 CRBN

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.3150842_3150845dup , CM000665.2:g.3150842_3150845dup	GRCh38
NC_000003.11:g.3192526_3192529dup , CM000665.1:g.3192526_3192529dup	GRCh37
NC_000003.10:g.3167526_3167529dup	NCBI36
NG_016864.1:g.33874_33877dup
NG_041800.1:g.28927_28930dup
NG_041800.2:g.28927_28930dup
NG_016864.2:g.33874_33877dup

Transcript Alleles

HGVS	Amino-acid Change
NM_016302.4:c.*21_*24dup (CRBN) MANE Select	NP_057386.2:n.*21_*24dup
ENST00000231948.9:c.*21_*24dup (CRBN) MANE Select	ENSP00000231948.4:n.*21_*24dup
NM_001173482.1:c.*21_*24dup (CRBN)	NP_001166953.1:n.*21_*24dup
NM_001367321.1:c.*336_*339dup (TRNT1)	NP_001354250.1:n.*336_*339dup
NM_016302.3:c.*21_*24dup (CRBN)	NP_057386.2:n.*21_*24dup
NR_159934.1:n.1859_1862dup (TRNT1)
NR_159935.1:n.1557-1572_1557-1569dup (TRNT1)
NR_159936.1:n.1665_1668dup (TRNT1)
NR_159937.1:n.2901_2904dup (TRNT1)
ENST00000231948.8:c.*21_*24dup (CRBN)	ENSP00000231948.4:n.*21_*24dup
ENST00000424814.5:c.1205_1208dup (CRBN)
ENST00000432408.6:c.*21_*24dup (CRBN)	ENSP00000412499.2:n.*21_*24dup
ENST00000434583.5:c.*476_*479dup (TRNT1)	ENSP00000415100.1:n.*476_*479dup
ENST00000488263.5:n.3695_3698dup (CRBN)
ENST00000491834.5:n.3776_3779dup (CRBN)
ENST00000639284.1:c.1311+39_1311+42dup (CRBN)	ENSP00000491442.1:n.1311+39_1311+42dup
ENST00000698406.1:c.*34-1572_*34-1569dup (TRNT1)	ENSP00000513700.1:n.*34-1572_*34-1569dup
ENST00000698407.1:n.4622_4625dup (TRNT1)
ENST00000698408.1:c.*174-1572_*174-1569dup (TRNT1)	ENSP00000513701.1:n.*174-1572_*174-1569dup
ENST00000698410.1:c.*3464_*3467dup (TRNT1)	ENSP00000513703.1:n.*3464_*3467dup
ENST00000698412.1:c.*2688_*2691dup (TRNT1)	ENSP00000513705.1:n.*2688_*2691dup
ENST00000698413.1:c.*2688_*2691dup (TRNT1)	ENSP00000513706.1:n.*2688_*2691dup
ENST00000698414.1:c.*2688_*2691dup (TRNT1)	ENSP00000513707.1:n.*2688_*2691dup
ENST00000698415.1:n.5354_5357dup (TRNT1)
ENST00000698416.1:n.4257_4260dup (TRNT1)
XM_005265202.2:c.*21_*24dup (CRBN)	XP_005265259.1:n.*21_*24dup
XM_005265202.4:c.*21_*24dup (CRBN)	XP_005265259.1:n.*21_*24dup
XM_011533778.3:c.*336_*339dup (TRNT1)	XP_011532080.1:n.*336_*339dup
XM_011533791.1:c.*21_*24dup (CRBN)	XP_011532093.1:n.*21_*24dup
XM_011533791.3:c.*21_*24dup (CRBN)	XP_011532093.1:n.*21_*24dup
XM_011533793.1:c.*21_*24dup (CRBN)	XP_011532095.1:n.*21_*24dup
XM_011533793.2:c.*21_*24dup (CRBN)	XP_011532095.1:n.*21_*24dup
XM_011533794.1:c.*21_*24dup (CRBN)	XP_011532096.1:n.*21_*24dup
XM_011533794.2:c.*21_*24dup (CRBN)	XP_011532096.1:n.*21_*24dup
XM_024453551.1:c.*247_*250dup (CRBN)	XP_024309319.1:n.*247_*250dup
XR_001740169.2:n.2466-1572_2466-1569dup (TRNT1)
XR_940445.3:n.1862_1865dup (TRNT1)
XR_940446.1:n.1581-1572_1581-1569dup (TRNT1)
XR_940446.3:n.1560-1572_1560-1569dup (TRNT1)
XR_940448.1:n.1251_1254dup (CRBN)
XR_940448.3:n.1248_1251dup (CRBN)