Canonical Allele Identifier: CA2486499856
Gene: TBCE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.235438760T= , CM000663.2:g.235438760T= GRCh38
NC_000001.10:g.235602075T= , CM000663.1:g.235602075T= GRCh37
NC_000001.9:g.233668698T= NCBI36
NG_009230.1:g.76348T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000366601.8:c.928-9T= ENSP00000355560.4:n.928-9T=
ENST00000406207.5:c.1117-9T= ENSP00000384571.1:n.1117-9T=
ENST00000472011.6:n.1841-9T=
ENST00000543662.4:c.1270-9T= ENSP00000439170.1:n.1270-9T=
ENST00000642339.1:c.*814-9T= ENSP00000495425.1:n.*814-9T=
ENST00000642431.1:c.1694-9T=
ENST00000642463.1:c.*1015-9T= ENSP00000495007.1:n.*1015-9T=
ENST00000642503.1:c.*891-9T= ENSP00000494334.1:n.*891-9T=
ENST00000642610.2:c.1117-9T= MANE Select ENSP00000494796.1:n.1117-9T=
ENST00000642764.1:n.1948-9T=
ENST00000643125.1:c.*132-9T= ENSP00000494102.1:n.*132-9T=
ENST00000643142.1:c.*608-9T= ENSP00000494755.1:n.*608-9T=
ENST00000643238.1:c.*137-9T= ENSP00000495916.1:n.*137-9T=
ENST00000643410.1:c.*407-9T= ENSP00000495030.1:n.*407-9T=
ENST00000643487.1:n.1804-9T=
ENST00000643524.1:c.*702-9T= ENSP00000494026.1:n.*702-9T=
ENST00000643615.1:c.*1116+1286T= ENSP00000496103.1:n.*1116+1286T=
ENST00000643993.1:n.1253-9T=
ENST00000643994.1:c.*1117-9T= ENSP00000496322.1:n.*1117-9T=
ENST00000644037.1:c.*1327-9T= ENSP00000496408.1:n.*1327-9T=
ENST00000644055.1:c.*1742-9T= ENSP00000496307.1:n.*1742-9T=
ENST00000644126.1:n.2789-9T=
ENST00000644217.1:c.1117-9T= ENSP00000494646.1:n.1117-9T=
ENST00000644265.1:c.486-9T=
ENST00000644578.1:c.931-9T= ENSP00000495953.1:n.931-9T=
ENST00000644604.1:c.1117-9T= ENSP00000495961.1:n.1117-9T=
ENST00000644680.1:c.*1638-9T= ENSP00000496173.1:n.*1638-9T=
ENST00000644838.1:c.*500-9T= ENSP00000495910.1:n.*500-9T=
ENST00000644910.1:c.1724-9T=
ENST00000645205.1:c.1117-9T= ENSP00000495823.1:n.1117-9T=
ENST00000645351.1:c.1117-9T= ENSP00000494319.1:n.1117-9T=
ENST00000645551.1:c.*834-9T= ENSP00000495928.1:n.*834-9T=
ENST00000645578.1:c.*891-9T= ENSP00000496495.1:n.*891-9T=
ENST00000645582.1:c.*947-9T= ENSP00000494980.1:n.*947-9T=
ENST00000645655.1:c.1117-9T= ENSP00000495202.1:n.1117-9T=
ENST00000645662.1:c.*576-9T= ENSP00000495964.1:n.*576-9T=
ENST00000645836.1:c.*891-9T= ENSP00000493915.1:n.*891-9T=
ENST00000645899.1:c.1117-9T= ENSP00000496773.1:n.1117-9T=
ENST00000645964.1:c.*983-9T= ENSP00000494208.1:n.*983-9T=
ENST00000646104.1:c.*1585-9T= ENSP00000495475.1:n.*1585-9T=
ENST00000646186.1:c.*789-9T= ENSP00000493806.1:n.*789-9T=
ENST00000646286.1:c.*1010-9T= ENSP00000494291.1:n.*1010-9T=
ENST00000646463.1:c.*882-9T= ENSP00000494541.1:n.*882-9T=
ENST00000646528.1:c.*1833-9T= ENSP00000496553.1:n.*1833-9T=
ENST00000646536.1:c.*407-9T= ENSP00000494801.1:n.*407-9T=
ENST00000646624.1:c.1117-9T= ENSP00000494575.1:n.1117-9T=
ENST00000646821.1:c.*407-9T= ENSP00000495257.1:n.*407-9T=
ENST00000646842.1:n.561-9T=
ENST00000646848.1:c.*332-9T= ENSP00000495831.1:n.*332-9T=
ENST00000647186.1:c.1117-9T= ENSP00000494775.1:n.1117-9T=
ENST00000647233.1:n.2097-9T=
ENST00000647322.1:c.708-9T=
ENST00000647418.1:c.*891-9T= ENSP00000493552.1:n.*891-9T=
ENST00000647428.1:c.778-9T= ENSP00000495630.1:n.778-9T=
ENST00000651186.1:c.778-9T= ENSP00000498645.1:n.778-9T=
ENST00000366601.7:c.1117-9T= ENSP00000355560.3:n.1117-9T=
ENST00000406207.4:c.1117-9T= ENSP00000384571.1:n.1117-9T=
ENST00000472011.5:n.1169-9T=
ENST00000543662.3:c.1270-9T= ENSP00000439170.1:n.1270-9T=
NM_001079515.2:c.1117-9T= NP_001072983.1:n.1117-9T=
NM_001287801.1:c.1270-9T= NP_001274730.1:n.1270-9T=
NM_001287802.1:c.778-9T= NP_001274731.1:n.778-9T=
NM_003193.4:c.1117-9T= NP_003184.1:n.1117-9T=
NM_003193.5:c.1117-9T= MANE Select NP_003184.1:n.1117-9T=
NM_001079515.3:c.1117-9T= NP_001072983.1:n.1117-9T=
NM_001287801.2:c.1270-9T= NP_001274730.1:n.1270-9T=
NM_001287802.2:c.778-9T= NP_001274731.1:n.778-9T=