Canonical Allele Identifier: CA2486499884
Gene: TBCE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.235438832A= , CM000663.2:g.235438832A= GRCh38
NC_000001.10:g.235602147A= , CM000663.1:g.235602147A= GRCh37
NC_000001.9:g.233668770A= NCBI36
NG_009230.1:g.76420A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000366601.8:c.991A= ENSP00000355560.4:p.Lys331=
ENST00000406207.5:c.1180A= ENSP00000384571.1:p.Lys394=
ENST00000472011.6:n.1904A=
ENST00000543662.4:c.1333A= ENSP00000439170.1:p.Lys445=
ENST00000642339.1:c.*877A= ENSP00000495425.1:n.*877A=
ENST00000642431.1:c.1757A=
ENST00000642463.1:c.*1078A= ENSP00000495007.1:n.*1078A=
ENST00000642503.1:c.*954A= ENSP00000494334.1:n.*954A=
ENST00000642610.2:c.1180A= MANE Select ENSP00000494796.1:p.Lys394=
ENST00000642764.1:n.2011A=
ENST00000643125.1:c.*195A= ENSP00000494102.1:n.*195A=
ENST00000643142.1:c.*671A= ENSP00000494755.1:n.*671A=
ENST00000643238.1:c.*200A= ENSP00000495916.1:n.*200A=
ENST00000643410.1:c.*470A= ENSP00000495030.1:n.*470A=
ENST00000643487.1:n.1867A=
ENST00000643524.1:c.*765A= ENSP00000494026.1:n.*765A=
ENST00000643615.1:c.*1116+1358A= ENSP00000496103.1:n.*1116+1358A=
ENST00000643993.1:n.1316A=
ENST00000643994.1:c.*1180A= ENSP00000496322.1:n.*1180A=
ENST00000644037.1:c.*1390A= ENSP00000496408.1:n.*1390A=
ENST00000644055.1:c.*1805A= ENSP00000496307.1:n.*1805A=
ENST00000644126.1:n.2852A=
ENST00000644217.1:c.1180A= ENSP00000494646.1:p.Lys394=
ENST00000644265.1:c.549A=
ENST00000644578.1:c.994A= ENSP00000495953.1:p.Lys332=
ENST00000644604.1:c.1180A= ENSP00000495961.1:p.Lys394=
ENST00000644680.1:c.*1701A= ENSP00000496173.1:n.*1701A=
ENST00000644838.1:c.*563A= ENSP00000495910.1:n.*563A=
ENST00000644910.1:c.1787A=
ENST00000645205.1:c.1180A= ENSP00000495823.1:p.Lys394=
ENST00000645351.1:c.1180A= ENSP00000494319.1:p.Lys394=
ENST00000645551.1:c.*897A= ENSP00000495928.1:n.*897A=
ENST00000645578.1:c.*954A= ENSP00000496495.1:n.*954A=
ENST00000645582.1:c.*1010A= ENSP00000494980.1:n.*1010A=
ENST00000645655.1:c.1180A= ENSP00000495202.1:p.Lys394=
ENST00000645662.1:c.*639A= ENSP00000495964.1:n.*639A=
ENST00000645836.1:c.*954A= ENSP00000493915.1:n.*954A=
ENST00000645899.1:c.1180A= ENSP00000496773.1:p.Lys394=
ENST00000645964.1:c.*1046A= ENSP00000494208.1:n.*1046A=
ENST00000646104.1:c.*1648A= ENSP00000495475.1:n.*1648A=
ENST00000646186.1:c.*852A= ENSP00000493806.1:n.*852A=
ENST00000646286.1:c.*1073A= ENSP00000494291.1:n.*1073A=
ENST00000646463.1:c.*945A= ENSP00000494541.1:n.*945A=
ENST00000646528.1:c.*1896A= ENSP00000496553.1:n.*1896A=
ENST00000646536.1:c.*470A= ENSP00000494801.1:n.*470A=
ENST00000646624.1:c.1180A= ENSP00000494575.1:p.Lys394=
ENST00000646821.1:c.*470A= ENSP00000495257.1:n.*470A=
ENST00000646842.1:n.624A=
ENST00000646848.1:c.*395A= ENSP00000495831.1:n.*395A=
ENST00000647186.1:c.1180A= ENSP00000494775.1:p.Lys394=
ENST00000647233.1:n.2160A=
ENST00000647322.1:c.771A=
ENST00000647418.1:c.*954A= ENSP00000493552.1:n.*954A=
ENST00000647428.1:c.841A= ENSP00000495630.1:p.Lys281=
ENST00000651186.1:c.841A= ENSP00000498645.1:p.Lys281=
ENST00000366601.7:c.1180A= ENSP00000355560.3:p.Lys394=
ENST00000406207.4:c.1180A= ENSP00000384571.1:p.Lys394=
ENST00000472011.5:n.1232A=
ENST00000543662.3:c.1333A= ENSP00000439170.1:p.Lys445=
NM_001079515.2:c.1180A= NP_001072983.1:p.Lys394=
NM_001287801.1:c.1333A= NP_001274730.1:p.Lys445=
NM_001287802.1:c.841A= NP_001274731.1:p.Lys281=
NM_003193.4:c.1180A= NP_003184.1:p.Lys394=
NM_003193.5:c.1180A= MANE Select NP_003184.1:p.Lys394=
NM_001079515.3:c.1180A= NP_001072983.1:p.Lys394=
NM_001287801.2:c.1333A= NP_001274730.1:p.Lys445=
NM_001287802.2:c.841A= NP_001274731.1:p.Lys281=