Canonical Allele Identifier: CA2486499902
Gene: TBCE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.235438867C= , CM000663.2:g.235438867C= GRCh38
NC_000001.10:g.235602182C= , CM000663.1:g.235602182C= GRCh37
NC_000001.9:g.233668805C= NCBI36
NG_009230.1:g.76455C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000366601.8:c.1026C= ENSP00000355560.4:p.Asn342=
ENST00000406207.5:c.1215C= ENSP00000384571.1:p.Asn405=
ENST00000472011.6:n.1939C=
ENST00000543662.4:c.1368C= ENSP00000439170.1:p.Asn456=
ENST00000642339.1:c.*912C= ENSP00000495425.1:n.*912C=
ENST00000642431.1:c.1792C=
ENST00000642463.1:c.*1113C= ENSP00000495007.1:n.*1113C=
ENST00000642503.1:c.*989C= ENSP00000494334.1:n.*989C=
ENST00000642610.2:c.1215C= MANE Select ENSP00000494796.1:p.Asn405=
ENST00000642764.1:n.2046C=
ENST00000643125.1:c.*230C= ENSP00000494102.1:n.*230C=
ENST00000643142.1:c.*706C= ENSP00000494755.1:n.*706C=
ENST00000643238.1:c.*235C= ENSP00000495916.1:n.*235C=
ENST00000643410.1:c.*505C= ENSP00000495030.1:n.*505C=
ENST00000643487.1:n.1902C=
ENST00000643524.1:c.*800C= ENSP00000494026.1:n.*800C=
ENST00000643615.1:c.*1116+1393C= ENSP00000496103.1:n.*1116+1393C=
ENST00000643993.1:n.1351C=
ENST00000643994.1:c.*1215C= ENSP00000496322.1:n.*1215C=
ENST00000644037.1:c.*1425C= ENSP00000496408.1:n.*1425C=
ENST00000644055.1:c.*1840C= ENSP00000496307.1:n.*1840C=
ENST00000644126.1:n.2887C=
ENST00000644217.1:c.1215C= ENSP00000494646.1:p.Asn405=
ENST00000644265.1:c.584C=
ENST00000644578.1:c.1029C= ENSP00000495953.1:p.Asn343=
ENST00000644604.1:c.1215C= ENSP00000495961.1:p.Asn405=
ENST00000644680.1:c.*1736C= ENSP00000496173.1:n.*1736C=
ENST00000644838.1:c.*598C= ENSP00000495910.1:n.*598C=
ENST00000644910.1:c.1822C=
ENST00000645205.1:c.1215C= ENSP00000495823.1:p.Asn405=
ENST00000645351.1:c.1215C= ENSP00000494319.1:p.Asn405=
ENST00000645551.1:c.*932C= ENSP00000495928.1:n.*932C=
ENST00000645578.1:c.*989C= ENSP00000496495.1:n.*989C=
ENST00000645582.1:c.*1045C= ENSP00000494980.1:n.*1045C=
ENST00000645655.1:c.1215C= ENSP00000495202.1:p.Asn405=
ENST00000645662.1:c.*674C= ENSP00000495964.1:n.*674C=
ENST00000645836.1:c.*989C= ENSP00000493915.1:n.*989C=
ENST00000645899.1:c.1215C= ENSP00000496773.1:p.Asn405=
ENST00000645964.1:c.*1081C= ENSP00000494208.1:n.*1081C=
ENST00000646104.1:c.*1683C= ENSP00000495475.1:n.*1683C=
ENST00000646186.1:c.*887C= ENSP00000493806.1:n.*887C=
ENST00000646286.1:c.*1108C= ENSP00000494291.1:n.*1108C=
ENST00000646463.1:c.*980C= ENSP00000494541.1:n.*980C=
ENST00000646528.1:c.*1931C= ENSP00000496553.1:n.*1931C=
ENST00000646536.1:c.*505C= ENSP00000494801.1:n.*505C=
ENST00000646624.1:c.1215C= ENSP00000494575.1:p.Asn405=
ENST00000646821.1:c.*505C= ENSP00000495257.1:n.*505C=
ENST00000646842.1:n.659C=
ENST00000646848.1:c.*430C= ENSP00000495831.1:n.*430C=
ENST00000647186.1:c.1215C= ENSP00000494775.1:p.Asn405=
ENST00000647233.1:n.2195C=
ENST00000647322.1:c.806C=
ENST00000647418.1:c.*989C= ENSP00000493552.1:n.*989C=
ENST00000647428.1:c.876C= ENSP00000495630.1:p.Asn292=
ENST00000651186.1:c.876C= ENSP00000498645.1:p.Asn292=
ENST00000366601.7:c.1215C= ENSP00000355560.3:p.Asn405=
ENST00000406207.4:c.1215C= ENSP00000384571.1:p.Asn405=
ENST00000472011.5:n.1267C=
ENST00000543662.3:c.1368C= ENSP00000439170.1:p.Asn456=
NM_001079515.2:c.1215C= NP_001072983.1:p.Asn405=
NM_001287801.1:c.1368C= NP_001274730.1:p.Asn456=
NM_001287802.1:c.876C= NP_001274731.1:p.Asn292=
NM_003193.4:c.1215C= NP_003184.1:p.Asn405=
NM_003193.5:c.1215C= MANE Select NP_003184.1:p.Asn405=
NM_001079515.3:c.1215C= NP_001072983.1:p.Asn405=
NM_001287801.2:c.1368C= NP_001274730.1:p.Asn456=
NM_001287802.2:c.876C= NP_001274731.1:p.Asn292=