Canonical Allele Identifier: CA2486499905
Gene: TBCE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.235438886C= , CM000663.2:g.235438886C= GRCh38
NC_000001.10:g.235602201C= , CM000663.1:g.235602201C= GRCh37
NC_000001.9:g.233668824C= NCBI36
NG_009230.1:g.76474C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000366601.8:c.1045C= ENSP00000355560.4:p.Leu349=
ENST00000406207.5:c.1234C= ENSP00000384571.1:p.Leu412=
ENST00000472011.6:n.1958C=
ENST00000543662.4:c.1387C= ENSP00000439170.1:p.Leu463=
ENST00000642339.1:c.*931C= ENSP00000495425.1:n.*931C=
ENST00000642431.1:c.1811C=
ENST00000642463.1:c.*1132C= ENSP00000495007.1:n.*1132C=
ENST00000642503.1:c.*1008C= ENSP00000494334.1:n.*1008C=
ENST00000642610.2:c.1234C= MANE Select ENSP00000494796.1:p.Leu412=
ENST00000642764.1:n.2065C=
ENST00000643125.1:c.*249C= ENSP00000494102.1:n.*249C=
ENST00000643142.1:c.*725C= ENSP00000494755.1:n.*725C=
ENST00000643238.1:c.*254C= ENSP00000495916.1:n.*254C=
ENST00000643410.1:c.*524C= ENSP00000495030.1:n.*524C=
ENST00000643487.1:n.1921C=
ENST00000643524.1:c.*819C= ENSP00000494026.1:n.*819C=
ENST00000643615.1:c.*1116+1412C= ENSP00000496103.1:n.*1116+1412C=
ENST00000643993.1:n.1370C=
ENST00000643994.1:c.*1234C= ENSP00000496322.1:n.*1234C=
ENST00000644037.1:c.*1444C= ENSP00000496408.1:n.*1444C=
ENST00000644055.1:c.*1859C= ENSP00000496307.1:n.*1859C=
ENST00000644126.1:n.2906C=
ENST00000644217.1:c.1234C= ENSP00000494646.1:p.Leu412=
ENST00000644265.1:c.603C=
ENST00000644578.1:c.1048C= ENSP00000495953.1:p.Leu350=
ENST00000644604.1:c.1234C= ENSP00000495961.1:p.Leu412=
ENST00000644680.1:c.*1755C= ENSP00000496173.1:n.*1755C=
ENST00000644838.1:c.*617C= ENSP00000495910.1:n.*617C=
ENST00000644910.1:c.1841C=
ENST00000645205.1:c.1234C= ENSP00000495823.1:p.Leu412=
ENST00000645351.1:c.1234C= ENSP00000494319.1:p.Leu412=
ENST00000645551.1:c.*951C= ENSP00000495928.1:n.*951C=
ENST00000645578.1:c.*1008C= ENSP00000496495.1:n.*1008C=
ENST00000645582.1:c.*1064C= ENSP00000494980.1:n.*1064C=
ENST00000645655.1:c.1234C= ENSP00000495202.1:p.Leu412=
ENST00000645662.1:c.*693C= ENSP00000495964.1:n.*693C=
ENST00000645836.1:c.*1008C= ENSP00000493915.1:n.*1008C=
ENST00000645899.1:c.1234C= ENSP00000496773.1:p.Leu412=
ENST00000645964.1:c.*1100C= ENSP00000494208.1:n.*1100C=
ENST00000646104.1:c.*1702C= ENSP00000495475.1:n.*1702C=
ENST00000646186.1:c.*906C= ENSP00000493806.1:n.*906C=
ENST00000646286.1:c.*1127C= ENSP00000494291.1:n.*1127C=
ENST00000646463.1:c.*999C= ENSP00000494541.1:n.*999C=
ENST00000646528.1:c.*1950C= ENSP00000496553.1:n.*1950C=
ENST00000646536.1:c.*524C= ENSP00000494801.1:n.*524C=
ENST00000646624.1:c.1234C= ENSP00000494575.1:p.Leu412=
ENST00000646821.1:c.*524C= ENSP00000495257.1:n.*524C=
ENST00000646842.1:n.678C=
ENST00000646848.1:c.*449C= ENSP00000495831.1:n.*449C=
ENST00000647186.1:c.1234C= ENSP00000494775.1:p.Leu412=
ENST00000647233.1:n.2214C=
ENST00000647322.1:c.825C=
ENST00000647418.1:c.*1008C= ENSP00000493552.1:n.*1008C=
ENST00000647428.1:c.895C= ENSP00000495630.1:p.Leu299=
ENST00000651186.1:c.895C= ENSP00000498645.1:p.Leu299=
ENST00000366601.7:c.1234C= ENSP00000355560.3:p.Leu412=
ENST00000406207.4:c.1234C= ENSP00000384571.1:p.Leu412=
ENST00000472011.5:n.1286C=
ENST00000543662.3:c.1387C= ENSP00000439170.1:p.Leu463=
NM_001079515.2:c.1234C= NP_001072983.1:p.Leu412=
NM_001287801.1:c.1387C= NP_001274730.1:p.Leu463=
NM_001287802.1:c.895C= NP_001274731.1:p.Leu299=
NM_003193.4:c.1234C= NP_003184.1:p.Leu412=
NM_003193.5:c.1234C= MANE Select NP_003184.1:p.Leu412=
NM_001079515.3:c.1234C= NP_001072983.1:p.Leu412=
NM_001287801.2:c.1387C= NP_001274730.1:p.Leu463=
NM_001287802.2:c.895C= NP_001274731.1:p.Leu299=