Canonical Allele Identifier: CA2486499911
Gene: TBCE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.235438913C= , CM000663.2:g.235438913C= GRCh38
NC_000001.10:g.235602228C= , CM000663.1:g.235602228C= GRCh37
NC_000001.9:g.233668851C= NCBI36
NG_009230.1:g.76501C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000366601.8:c.1072C= ENSP00000355560.4:p.Leu358=
ENST00000406207.5:c.1261C= ENSP00000384571.1:p.Leu421=
ENST00000472011.6:n.1985C=
ENST00000543662.4:c.1414C= ENSP00000439170.1:p.Leu472=
ENST00000642339.1:c.*958C= ENSP00000495425.1:n.*958C=
ENST00000642431.1:c.1838C=
ENST00000642463.1:c.*1159C= ENSP00000495007.1:n.*1159C=
ENST00000642503.1:c.*1035C= ENSP00000494334.1:n.*1035C=
ENST00000642610.2:c.1261C= MANE Select ENSP00000494796.1:p.Leu421=
ENST00000642764.1:n.2092C=
ENST00000643125.1:c.*276C= ENSP00000494102.1:n.*276C=
ENST00000643142.1:c.*752C= ENSP00000494755.1:n.*752C=
ENST00000643238.1:c.*281C= ENSP00000495916.1:n.*281C=
ENST00000643410.1:c.*551C= ENSP00000495030.1:n.*551C=
ENST00000643487.1:n.1948C=
ENST00000643524.1:c.*846C= ENSP00000494026.1:n.*846C=
ENST00000643615.1:c.*1116+1439C= ENSP00000496103.1:n.*1116+1439C=
ENST00000643993.1:n.1397C=
ENST00000643994.1:c.*1261C= ENSP00000496322.1:n.*1261C=
ENST00000644037.1:c.*1471C= ENSP00000496408.1:n.*1471C=
ENST00000644055.1:c.*1886C= ENSP00000496307.1:n.*1886C=
ENST00000644126.1:n.2933C=
ENST00000644217.1:c.1261C= ENSP00000494646.1:p.Leu421=
ENST00000644265.1:c.630C=
ENST00000644578.1:c.1075C= ENSP00000495953.1:p.Leu359=
ENST00000644604.1:c.1261C= ENSP00000495961.1:p.Leu421=
ENST00000644680.1:c.*1782C= ENSP00000496173.1:n.*1782C=
ENST00000644838.1:c.*644C= ENSP00000495910.1:n.*644C=
ENST00000644910.1:c.1868C=
ENST00000645205.1:c.1261C= ENSP00000495823.1:p.Leu421=
ENST00000645351.1:c.1261C= ENSP00000494319.1:p.Leu421=
ENST00000645551.1:c.*978C= ENSP00000495928.1:n.*978C=
ENST00000645578.1:c.*1035C= ENSP00000496495.1:n.*1035C=
ENST00000645582.1:c.*1091C= ENSP00000494980.1:n.*1091C=
ENST00000645655.1:c.1261C= ENSP00000495202.1:p.Leu421=
ENST00000645836.1:c.*1035C= ENSP00000493915.1:n.*1035C=
ENST00000645899.1:c.1261C= ENSP00000496773.1:p.Leu421=
ENST00000645964.1:c.*1127C= ENSP00000494208.1:n.*1127C=
ENST00000646104.1:c.*1729C= ENSP00000495475.1:n.*1729C=
ENST00000646186.1:c.*933C= ENSP00000493806.1:n.*933C=
ENST00000646286.1:c.*1154C= ENSP00000494291.1:n.*1154C=
ENST00000646463.1:c.*1026C= ENSP00000494541.1:n.*1026C=
ENST00000646528.1:c.*1977C= ENSP00000496553.1:n.*1977C=
ENST00000646536.1:c.*551C= ENSP00000494801.1:n.*551C=
ENST00000646624.1:c.1261C= ENSP00000494575.1:p.Leu421=
ENST00000646821.1:c.*551C= ENSP00000495257.1:n.*551C=
ENST00000646842.1:n.705C=
ENST00000646848.1:c.*476C= ENSP00000495831.1:n.*476C=
ENST00000647186.1:c.1261C= ENSP00000494775.1:p.Leu421=
ENST00000647233.1:n.2241C=
ENST00000647322.1:c.852C=
ENST00000647418.1:c.*1035C= ENSP00000493552.1:n.*1035C=
ENST00000647428.1:c.922C= ENSP00000495630.1:p.Leu308=
ENST00000651186.1:c.922C= ENSP00000498645.1:p.Leu308=
ENST00000366601.7:c.1261C= ENSP00000355560.3:p.Leu421=
ENST00000406207.4:c.1261C= ENSP00000384571.1:p.Leu421=
ENST00000472011.5:n.1313C=
ENST00000543662.3:c.1414C= ENSP00000439170.1:p.Leu472=
NM_001079515.2:c.1261C= NP_001072983.1:p.Leu421=
NM_001287801.1:c.1414C= NP_001274730.1:p.Leu472=
NM_001287802.1:c.922C= NP_001274731.1:p.Leu308=
NM_003193.4:c.1261C= NP_003184.1:p.Leu421=
NM_003193.5:c.1261C= MANE Select NP_003184.1:p.Leu421=
NM_001079515.3:c.1261C= NP_001072983.1:p.Leu421=
NM_001287801.2:c.1414C= NP_001274730.1:p.Leu472=
NM_001287802.2:c.922C= NP_001274731.1:p.Leu308=