Canonical Allele Identifier: CA1142500086
Gene: TBCE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.235438769A= , CM000663.2:g.235438769A= GRCh38
NC_000001.10:g.235602084A= , CM000663.1:g.235602084A= GRCh37
NC_000001.9:g.233668707A= NCBI36
NG_009230.1:g.76357A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000366601.8:c.928A= ENSP00000355560.4:p.Ile310=
ENST00000406207.5:c.1117A= ENSP00000384571.1:p.Ile373=
ENST00000472011.6:n.1841A=
ENST00000543662.4:c.1270A= ENSP00000439170.1:p.Ile424=
ENST00000642339.1:c.*814A= ENSP00000495425.1:n.*814A=
ENST00000642431.1:c.1694A=
ENST00000642463.1:c.*1015A= ENSP00000495007.1:n.*1015A=
ENST00000642503.1:c.*891A= ENSP00000494334.1:n.*891A=
ENST00000642610.2:c.1117A= MANE Select ENSP00000494796.1:p.Ile373=
ENST00000642764.1:n.1948A=
ENST00000643125.1:c.*132A= ENSP00000494102.1:n.*132A=
ENST00000643142.1:c.*608A= ENSP00000494755.1:n.*608A=
ENST00000643238.1:c.*137A= ENSP00000495916.1:n.*137A=
ENST00000643410.1:c.*407A= ENSP00000495030.1:n.*407A=
ENST00000643487.1:n.1804A=
ENST00000643524.1:c.*702A= ENSP00000494026.1:n.*702A=
ENST00000643615.1:c.*1116+1295A= ENSP00000496103.1:n.*1116+1295A=
ENST00000643993.1:n.1253A=
ENST00000643994.1:c.*1117A= ENSP00000496322.1:n.*1117A=
ENST00000644037.1:c.*1327A= ENSP00000496408.1:n.*1327A=
ENST00000644055.1:c.*1742A= ENSP00000496307.1:n.*1742A=
ENST00000644126.1:n.2789A=
ENST00000644217.1:c.1117A= ENSP00000494646.1:p.Ile373=
ENST00000644265.1:c.486A=
ENST00000644578.1:c.931A= ENSP00000495953.1:p.Ile311=
ENST00000644604.1:c.1117A= ENSP00000495961.1:p.Ile373=
ENST00000644680.1:c.*1638A= ENSP00000496173.1:n.*1638A=
ENST00000644838.1:c.*500A= ENSP00000495910.1:n.*500A=
ENST00000644910.1:c.1724A=
ENST00000645205.1:c.1117A= ENSP00000495823.1:p.Ile373=
ENST00000645351.1:c.1117A= ENSP00000494319.1:p.Ile373=
ENST00000645551.1:c.*834A= ENSP00000495928.1:n.*834A=
ENST00000645578.1:c.*891A= ENSP00000496495.1:n.*891A=
ENST00000645582.1:c.*947A= ENSP00000494980.1:n.*947A=
ENST00000645655.1:c.1117A= ENSP00000495202.1:p.Ile373=
ENST00000645662.1:c.*576A= ENSP00000495964.1:n.*576A=
ENST00000645836.1:c.*891A= ENSP00000493915.1:n.*891A=
ENST00000645899.1:c.1117A= ENSP00000496773.1:p.Ile373=
ENST00000645964.1:c.*983A= ENSP00000494208.1:n.*983A=
ENST00000646104.1:c.*1585A= ENSP00000495475.1:n.*1585A=
ENST00000646186.1:c.*789A= ENSP00000493806.1:n.*789A=
ENST00000646286.1:c.*1010A= ENSP00000494291.1:n.*1010A=
ENST00000646463.1:c.*882A= ENSP00000494541.1:n.*882A=
ENST00000646528.1:c.*1833A= ENSP00000496553.1:n.*1833A=
ENST00000646536.1:c.*407A= ENSP00000494801.1:n.*407A=
ENST00000646624.1:c.1117A= ENSP00000494575.1:p.Ile373=
ENST00000646821.1:c.*407A= ENSP00000495257.1:n.*407A=
ENST00000646842.1:n.561A=
ENST00000646848.1:c.*332A= ENSP00000495831.1:n.*332A=
ENST00000647186.1:c.1117A= ENSP00000494775.1:p.Ile373=
ENST00000647233.1:n.2097A=
ENST00000647322.1:c.708A=
ENST00000647418.1:c.*891A= ENSP00000493552.1:n.*891A=
ENST00000647428.1:c.778A= ENSP00000495630.1:p.Ile260=
ENST00000651186.1:c.778A= ENSP00000498645.1:p.Ile260=
ENST00000366601.7:c.1117A= ENSP00000355560.3:p.Ile373=
ENST00000406207.4:c.1117A= ENSP00000384571.1:p.Ile373=
ENST00000472011.5:n.1169A=
ENST00000543662.3:c.1270A= ENSP00000439170.1:p.Ile424=
NM_001079515.2:c.1117A= NP_001072983.1:p.Ile373=
NM_001287801.1:c.1270A= NP_001274730.1:p.Ile424=
NM_001287802.1:c.778A= NP_001274731.1:p.Ile260=
NM_003193.4:c.1117A= NP_003184.1:p.Ile373=
NM_003193.5:c.1117A= MANE Select NP_003184.1:p.Ile373=
NM_001079515.3:c.1117A= NP_001072983.1:p.Ile373=
NM_001287801.2:c.1270A= NP_001274730.1:p.Ile424=
NM_001287802.2:c.778A= NP_001274731.1:p.Ile260=