Canonical Allele Identifier: CA2228936

Gene: TRNT1 CRBN

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.3148140A>G , CM000665.2:g.3148140A>G	GRCh38
NC_000003.11:g.3189824A>G , CM000665.1:g.3189824A>G	GRCh37
NC_000003.10:g.3164824A>G	NCBI36
NG_016864.1:g.36578T>C
NG_041800.1:g.26225A>G
NG_041800.2:g.26225A>G
NG_016864.2:g.36578T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698406.1:c.1291A>G (TRNT1)	ENSP00000513700.1:p.Ile431Val
ENST00000698407.1:n.1920A>G (TRNT1)
ENST00000698408.1:c.1291A>G (TRNT1)	ENSP00000513701.1:p.Ile431Val
ENST00000698410.1:c.*762A>G (TRNT1)	ENSP00000513703.1:n.*762A>G
ENST00000698412.1:c.1291A>G (TRNT1)	ENSP00000513705.1:p.Ile431Val
ENST00000698413.1:c.1408A>G (TRNT1)	ENSP00000513706.1:p.Ile470Val
ENST00000698414.1:c.1408A>G (TRNT1)	ENSP00000513707.1:p.Ile470Val
ENST00000698415.1:n.2652A>G (TRNT1)
ENST00000698416.1:n.1555A>G (TRNT1)
ENST00000251607.11:c.1291A>G (TRNT1) MANE Select	ENSP00000251607.6:p.Ile431Val
ENST00000639284.1:c.1312-2641T>C (CRBN)	ENSP00000491442.1:n.1312-2641T>C
ENST00000650755.1:c.*941A>G (TRNT1)	ENSP00000499122.1:n.*941A>G
ENST00000650814.1:c.991A>G (TRNT1)
ENST00000650839.1:c.*663A>G (TRNT1)	ENSP00000498970.1:n.*663A>G
ENST00000651316.1:c.*636A>G (TRNT1)	ENSP00000498787.1:n.*636A>G
ENST00000651591.1:c.*1021A>G (TRNT1)	ENSP00000498240.1:n.*1021A>G
ENST00000652340.1:c.1084A>G (TRNT1)	ENSP00000498624.1:n.1084A>G
ENST00000251607.10:c.1291A>G (TRNT1)	ENSP00000251607.6:p.Ile431Val
ENST00000280591.10:c.1231A>G (TRNT1)	ENSP00000280591.6:p.Ile411Val
ENST00000434583.5:c.1291A>G (TRNT1)	ENSP00000415100.1:p.Ile431Val
NM_001302946.1:c.1231A>G (TRNT1)	NP_001289875.1:p.Ile411Val
NM_182916.2:c.1291A>G (TRNT1)	NP_886552.2:p.Ile431Val
XM_005265196.1:c.1291A>G (TRNT1)	XP_005265253.1:p.Ile431Val
XM_011533776.1:c.1291A>G (TRNT1)	XP_011532078.1:p.Ile431Val
XM_011533777.1:c.1291A>G (TRNT1)	XP_011532079.1:p.Ile431Val
XM_011533778.1:c.1291A>G (TRNT1)	XP_011532080.1:p.Ile431Val
XR_940445.1:n.1393A>G (TRNT1)
XR_940446.1:n.1393A>G (TRNT1)
XM_011533776.3:c.1291A>G (TRNT1)	XP_011532078.1:p.Ile431Val
XM_011533777.2:c.1291A>G (TRNT1)	XP_011532079.1:p.Ile431Val
XM_011533778.3:c.1291A>G (TRNT1)	XP_011532080.1:p.Ile431Val
XR_001740168.2:n.1372A>G (TRNT1)
XR_001740169.2:n.1372A>G (TRNT1)
XR_940445.3:n.1372A>G (TRNT1)
XR_940446.3:n.1372A>G (TRNT1)
NM_001302946.2:c.1231A>G (TRNT1)	NP_001289875.2:p.Ile411Val
NM_001367321.1:c.1291A>G (TRNT1)	NP_001354250.1:p.Ile431Val
NM_001367322.1:c.1291A>G (TRNT1)	NP_001354251.1:p.Ile431Val
NM_001367323.1:c.1291A>G (TRNT1)	NP_001354252.1:p.Ile431Val
NM_182916.3:c.1291A>G (TRNT1) MANE Select	NP_886552.3:p.Ile431Val
NR_159934.1:n.1369A>G (TRNT1)
NR_159935.1:n.1369A>G (TRNT1)
NR_159936.1:n.1175A>G (TRNT1)
NR_159937.1:n.2411A>G (TRNT1)
NR_159938.1:n.1175A>G (TRNT1)
NR_159939.1:n.1230A>G (TRNT1)
NR_159940.1:n.1244A>G (TRNT1)
NR_159941.1:n.2411A>G (TRNT1)