Canonical Allele Identifier: CA2486499894

Gene: TBCE

Linked Data

• dbSNP Id: rs1681634799

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.235438851del , CM000663.2:g.235438851del	GRCh38
NC_000001.10:g.235602166del , CM000663.1:g.235602166del	GRCh37
NC_000001.9:g.233668789del	NCBI36
NG_009230.1:g.76439del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366601.8:c.1010del	ENSP00000355560.4:p.Lys337ArgfsTer24
ENST00000406207.5:c.1199del	ENSP00000384571.1:p.Lys400ArgfsTer24
ENST00000472011.6:n.1923del
ENST00000543662.4:c.1352del	ENSP00000439170.1:p.Lys451ArgfsTer24
ENST00000642339.1:c.*896del	ENSP00000495425.1:n.*896del
ENST00000642431.1:c.1776del
ENST00000642463.1:c.*1097del	ENSP00000495007.1:n.*1097del
ENST00000642503.1:c.*973del	ENSP00000494334.1:n.*973del
ENST00000642610.2:c.1199del MANE Select	ENSP00000494796.1:p.Lys400ArgfsTer24
ENST00000642764.1:n.2030del
ENST00000643125.1:c.*214del	ENSP00000494102.1:n.*214del
ENST00000643142.1:c.*690del	ENSP00000494755.1:n.*690del
ENST00000643238.1:c.*219del	ENSP00000495916.1:n.*219del
ENST00000643410.1:c.*489del	ENSP00000495030.1:n.*489del
ENST00000643487.1:n.1886del
ENST00000643524.1:c.*784del	ENSP00000494026.1:n.*784del
ENST00000643615.1:c.*1116+1377del	ENSP00000496103.1:n.*1116+1377del
ENST00000643993.1:n.1335del
ENST00000643994.1:c.*1199del	ENSP00000496322.1:n.*1199del
ENST00000644037.1:c.*1409del	ENSP00000496408.1:n.*1409del
ENST00000644055.1:c.*1824del	ENSP00000496307.1:n.*1824del
ENST00000644126.1:n.2871del
ENST00000644217.1:c.1199del	ENSP00000494646.1:p.Lys400ArgfsTer24
ENST00000644265.1:c.568del
ENST00000644578.1:c.1013del	ENSP00000495953.1:p.Lys338ArgfsTer24
ENST00000644604.1:c.1199del	ENSP00000495961.1:p.Lys400ArgfsTer24
ENST00000644680.1:c.*1720del	ENSP00000496173.1:n.*1720del
ENST00000644838.1:c.*582del	ENSP00000495910.1:n.*582del
ENST00000644910.1:c.1806del
ENST00000645205.1:c.1199del	ENSP00000495823.1:p.Lys400ArgfsTer24
ENST00000645351.1:c.1199del	ENSP00000494319.1:p.Lys400ArgfsTer24
ENST00000645551.1:c.*916del	ENSP00000495928.1:n.*916del
ENST00000645578.1:c.*973del	ENSP00000496495.1:n.*973del
ENST00000645582.1:c.*1029del	ENSP00000494980.1:n.*1029del
ENST00000645655.1:c.1199del	ENSP00000495202.1:p.Lys400ArgfsTer24
ENST00000645662.1:c.*658del	ENSP00000495964.1:n.*658del
ENST00000645836.1:c.*973del	ENSP00000493915.1:n.*973del
ENST00000645899.1:c.1199del	ENSP00000496773.1:p.Lys400ArgfsTer24
ENST00000645964.1:c.*1065del	ENSP00000494208.1:n.*1065del
ENST00000646104.1:c.*1667del	ENSP00000495475.1:n.*1667del
ENST00000646186.1:c.*871del	ENSP00000493806.1:n.*871del
ENST00000646286.1:c.*1092del	ENSP00000494291.1:n.*1092del
ENST00000646463.1:c.*964del	ENSP00000494541.1:n.*964del
ENST00000646528.1:c.*1915del	ENSP00000496553.1:n.*1915del
ENST00000646536.1:c.*489del	ENSP00000494801.1:n.*489del
ENST00000646624.1:c.1199del	ENSP00000494575.1:p.Lys400ArgfsTer24
ENST00000646821.1:c.*489del	ENSP00000495257.1:n.*489del
ENST00000646842.1:n.643del
ENST00000646848.1:c.*414del	ENSP00000495831.1:n.*414del
ENST00000647186.1:c.1199del	ENSP00000494775.1:p.Lys400ArgfsTer24
ENST00000647233.1:n.2179del
ENST00000647322.1:c.790del
ENST00000647418.1:c.*973del	ENSP00000493552.1:n.*973del
ENST00000647428.1:c.860del	ENSP00000495630.1:p.Lys287ArgfsTer24
ENST00000651186.1:c.860del	ENSP00000498645.1:p.Lys287ArgfsTer24
ENST00000366601.7:c.1199del	ENSP00000355560.3:p.Lys400ArgfsTer24
ENST00000406207.4:c.1199del	ENSP00000384571.1:p.Lys400ArgfsTer24
ENST00000472011.5:n.1251del
ENST00000543662.3:c.1352del	ENSP00000439170.1:p.Lys451ArgfsTer24
NM_001079515.2:c.1199del	NP_001072983.1:p.Lys400ArgfsTer24
NM_001287801.1:c.1352del	NP_001274730.1:p.Lys451ArgfsTer24
NM_001287802.1:c.860del	NP_001274731.1:p.Lys287ArgfsTer24
NM_003193.4:c.1199del	NP_003184.1:p.Lys400ArgfsTer24
NM_003193.5:c.1199del MANE Select	NP_003184.1:p.Lys400ArgfsTer24
NM_001079515.3:c.1199del	NP_001072983.1:p.Lys400ArgfsTer24
NM_001287801.2:c.1352del	NP_001274730.1:p.Lys451ArgfsTer24
NM_001287802.2:c.860del	NP_001274731.1:p.Lys287ArgfsTer24