Canonical Allele Identifier: CA2486499879
Gene: TBCE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.235438822A= , CM000663.2:g.235438822A= GRCh38
NC_000001.10:g.235602137A= , CM000663.1:g.235602137A= GRCh37
NC_000001.9:g.233668760A= NCBI36
NG_009230.1:g.76410A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000366601.8:c.981A= ENSP00000355560.4:p.Gly327=
ENST00000406207.5:c.1170A= ENSP00000384571.1:p.Gly390=
ENST00000472011.6:n.1894A=
ENST00000543662.4:c.1323A= ENSP00000439170.1:p.Gly441=
ENST00000642339.1:c.*867A= ENSP00000495425.1:n.*867A=
ENST00000642431.1:c.1747A=
ENST00000642463.1:c.*1068A= ENSP00000495007.1:n.*1068A=
ENST00000642503.1:c.*944A= ENSP00000494334.1:n.*944A=
ENST00000642610.2:c.1170A= MANE Select ENSP00000494796.1:p.Gly390=
ENST00000642764.1:n.2001A=
ENST00000643125.1:c.*185A= ENSP00000494102.1:n.*185A=
ENST00000643142.1:c.*661A= ENSP00000494755.1:n.*661A=
ENST00000643238.1:c.*190A= ENSP00000495916.1:n.*190A=
ENST00000643410.1:c.*460A= ENSP00000495030.1:n.*460A=
ENST00000643487.1:n.1857A=
ENST00000643524.1:c.*755A= ENSP00000494026.1:n.*755A=
ENST00000643615.1:c.*1116+1348A= ENSP00000496103.1:n.*1116+1348A=
ENST00000643993.1:n.1306A=
ENST00000643994.1:c.*1170A= ENSP00000496322.1:n.*1170A=
ENST00000644037.1:c.*1380A= ENSP00000496408.1:n.*1380A=
ENST00000644055.1:c.*1795A= ENSP00000496307.1:n.*1795A=
ENST00000644126.1:n.2842A=
ENST00000644217.1:c.1170A= ENSP00000494646.1:p.Gly390=
ENST00000644265.1:c.539A=
ENST00000644578.1:c.984A= ENSP00000495953.1:p.Gly328=
ENST00000644604.1:c.1170A= ENSP00000495961.1:p.Gly390=
ENST00000644680.1:c.*1691A= ENSP00000496173.1:n.*1691A=
ENST00000644838.1:c.*553A= ENSP00000495910.1:n.*553A=
ENST00000644910.1:c.1777A=
ENST00000645205.1:c.1170A= ENSP00000495823.1:p.Gly390=
ENST00000645351.1:c.1170A= ENSP00000494319.1:p.Gly390=
ENST00000645551.1:c.*887A= ENSP00000495928.1:n.*887A=
ENST00000645578.1:c.*944A= ENSP00000496495.1:n.*944A=
ENST00000645582.1:c.*1000A= ENSP00000494980.1:n.*1000A=
ENST00000645655.1:c.1170A= ENSP00000495202.1:p.Gly390=
ENST00000645662.1:c.*629A= ENSP00000495964.1:n.*629A=
ENST00000645836.1:c.*944A= ENSP00000493915.1:n.*944A=
ENST00000645899.1:c.1170A= ENSP00000496773.1:p.Gly390=
ENST00000645964.1:c.*1036A= ENSP00000494208.1:n.*1036A=
ENST00000646104.1:c.*1638A= ENSP00000495475.1:n.*1638A=
ENST00000646186.1:c.*842A= ENSP00000493806.1:n.*842A=
ENST00000646286.1:c.*1063A= ENSP00000494291.1:n.*1063A=
ENST00000646463.1:c.*935A= ENSP00000494541.1:n.*935A=
ENST00000646528.1:c.*1886A= ENSP00000496553.1:n.*1886A=
ENST00000646536.1:c.*460A= ENSP00000494801.1:n.*460A=
ENST00000646624.1:c.1170A= ENSP00000494575.1:p.Gly390=
ENST00000646821.1:c.*460A= ENSP00000495257.1:n.*460A=
ENST00000646842.1:n.614A=
ENST00000646848.1:c.*385A= ENSP00000495831.1:n.*385A=
ENST00000647186.1:c.1170A= ENSP00000494775.1:p.Gly390=
ENST00000647233.1:n.2150A=
ENST00000647322.1:c.761A=
ENST00000647418.1:c.*944A= ENSP00000493552.1:n.*944A=
ENST00000647428.1:c.831A= ENSP00000495630.1:p.Gly277=
ENST00000651186.1:c.831A= ENSP00000498645.1:p.Gly277=
ENST00000366601.7:c.1170A= ENSP00000355560.3:p.Gly390=
ENST00000406207.4:c.1170A= ENSP00000384571.1:p.Gly390=
ENST00000472011.5:n.1222A=
ENST00000543662.3:c.1323A= ENSP00000439170.1:p.Gly441=
NM_001079515.2:c.1170A= NP_001072983.1:p.Gly390=
NM_001287801.1:c.1323A= NP_001274730.1:p.Gly441=
NM_001287802.1:c.831A= NP_001274731.1:p.Gly277=
NM_003193.4:c.1170A= NP_003184.1:p.Gly390=
NM_003193.5:c.1170A= MANE Select NP_003184.1:p.Gly390=
NM_001079515.3:c.1170A= NP_001072983.1:p.Gly390=
NM_001287801.2:c.1323A= NP_001274730.1:p.Gly441=
NM_001287802.2:c.831A= NP_001274731.1:p.Gly277=