Canonical Allele Identifier: CA2228709

Gene: TRNT1 CRBN

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.3144644_3144647del , CM000665.2:g.3144644_3144647del	GRCh38
NC_000003.11:g.3186328_3186331del , CM000665.1:g.3186328_3186331del	GRCh37
NC_000003.10:g.3161328_3161331del	NCBI36
NG_041800.1:g.22729_22732del
NG_041800.2:g.22729_22732del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698406.1:c.542_545del (TRNT1)	ENSP00000513700.1:p.Val181AspfsTer18
ENST00000698407.1:n.1171_1174del (TRNT1)
ENST00000698408.1:c.542_545del (TRNT1)	ENSP00000513701.1:p.Val181AspfsTer18
ENST00000698409.1:n.609_612del (TRNT1)
ENST00000698410.1:c.*13_*16del (TRNT1)	ENSP00000513703.1:n.*13_*16del
ENST00000698412.1:c.542_545del (TRNT1)	ENSP00000513705.1:p.Val181AspfsTer18
ENST00000698413.1:c.659_662del (TRNT1)	ENSP00000513706.1:p.Val220AspfsTer18
ENST00000698414.1:c.659_662del (TRNT1)	ENSP00000513707.1:p.Val220AspfsTer18
ENST00000698415.1:n.1903_1906del (TRNT1)
ENST00000251607.11:c.542_545del (TRNT1) MANE Select	ENSP00000251607.6:p.Val181AspfsTer18
ENST00000639284.1:c.*693_*696del (CRBN)	ENSP00000491442.1:n.*693_*696del
ENST00000650755.1:c.*192_*195del (TRNT1)	ENSP00000499122.1:n.*192_*195del
ENST00000650814.1:c.228_231del (TRNT1)
ENST00000650839.1:c.542_545del (TRNT1)	ENSP00000498970.1:p.Val181AspfsTer18
ENST00000650989.1:n.283_286del (TRNT1)
ENST00000651093.1:c.542_545del (TRNT1)	ENSP00000498942.1:p.Val181AspfsTer18
ENST00000651316.1:c.*81_*84del (TRNT1)	ENSP00000498787.1:n.*81_*84del
ENST00000651352.1:c.*13_*16del (TRNT1)	ENSP00000498449.1:n.*13_*16del
ENST00000651591.1:c.*466_*469del (TRNT1)	ENSP00000498240.1:n.*466_*469del
ENST00000652340.1:c.335_338del (TRNT1)	ENSP00000498624.1:n.335_338del
ENST00000251607.10:c.542_545del (TRNT1)	ENSP00000251607.6:p.Val181AspfsTer18
ENST00000280591.10:c.542_545del (TRNT1)	ENSP00000280591.6:p.Val181AspfsTer18
ENST00000434583.5:c.542_545del (TRNT1)	ENSP00000415100.1:p.Val181AspfsTer18
NM_001302946.1:c.542_545del (TRNT1)	NP_001289875.1:p.Val181AspfsTer18
NM_182916.2:c.542_545del (TRNT1)	NP_886552.2:p.Val181AspfsTer18
XM_005265196.1:c.542_545del (TRNT1)	XP_005265253.1:p.Val181AspfsTer18
XM_011533776.1:c.542_545del (TRNT1)	XP_011532078.1:p.Val181AspfsTer18
XM_011533777.1:c.542_545del (TRNT1)	XP_011532079.1:p.Val181AspfsTer18
XM_011533778.1:c.542_545del (TRNT1)	XP_011532080.1:p.Val181AspfsTer18
XR_940445.1:n.644_647del (TRNT1)
XR_940446.1:n.644_647del (TRNT1)
XM_011533776.3:c.542_545del (TRNT1)	XP_011532078.1:p.Val181AspfsTer18
XM_011533777.2:c.542_545del (TRNT1)	XP_011532079.1:p.Val181AspfsTer18
XM_011533778.3:c.542_545del (TRNT1)	XP_011532080.1:p.Val181AspfsTer18
XR_001740168.2:n.623_626del (TRNT1)
XR_001740169.2:n.623_626del (TRNT1)
XR_940445.3:n.623_626del (TRNT1)
XR_940446.3:n.623_626del (TRNT1)
NM_001302946.2:c.542_545del (TRNT1)	NP_001289875.2:p.Val181AspfsTer18
NM_001367321.1:c.542_545del (TRNT1)	NP_001354250.1:p.Val181AspfsTer18
NM_001367322.1:c.542_545del (TRNT1)	NP_001354251.1:p.Val181AspfsTer18
NM_001367323.1:c.542_545del (TRNT1)	NP_001354252.1:p.Val181AspfsTer18
NM_182916.3:c.542_545del (TRNT1) MANE Select	NP_886552.3:p.Val181AspfsTer18
NR_159934.1:n.620_623del (TRNT1)
NR_159935.1:n.620_623del (TRNT1)
NR_159936.1:n.620_623del (TRNT1)
NR_159937.1:n.1648_1651del (TRNT1)
NR_159938.1:n.620_623del (TRNT1)
NR_159939.1:n.481_484del (TRNT1)
NR_159940.1:n.481_484del (TRNT1)
NR_159941.1:n.1648_1651del (TRNT1)