Canonical Allele Identifier: CA344945221
Gene: TBCE HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.235438844G>C , CM000663.2:g.235438844G>C GRCh38
NC_000001.10:g.235602159G>C , CM000663.1:g.235602159G>C GRCh37
NC_000001.9:g.233668782G>C NCBI36
NG_009230.1:g.76432G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000366601.8:c.1003G>C ENSP00000355560.4:p.Gly335Arg
ENST00000406207.5:c.1192G>C ENSP00000384571.1:p.Gly398Arg
ENST00000472011.6:n.1916G>C
ENST00000543662.4:c.1345G>C ENSP00000439170.1:p.Gly449Arg
ENST00000642339.1:c.*889G>C ENSP00000495425.1:n.*889G>C
ENST00000642431.1:c.1769G>C
ENST00000642463.1:c.*1090G>C ENSP00000495007.1:n.*1090G>C
ENST00000642503.1:c.*966G>C ENSP00000494334.1:n.*966G>C
ENST00000642610.2:c.1192G>C MANE Select ENSP00000494796.1:p.Gly398Arg
ENST00000642764.1:n.2023G>C
ENST00000643125.1:c.*207G>C ENSP00000494102.1:n.*207G>C
ENST00000643142.1:c.*683G>C ENSP00000494755.1:n.*683G>C
ENST00000643238.1:c.*212G>C ENSP00000495916.1:n.*212G>C
ENST00000643410.1:c.*482G>C ENSP00000495030.1:n.*482G>C
ENST00000643487.1:n.1879G>C
ENST00000643524.1:c.*777G>C ENSP00000494026.1:n.*777G>C
ENST00000643615.1:c.*1116+1370G>C ENSP00000496103.1:n.*1116+1370G>C
ENST00000643993.1:n.1328G>C
ENST00000643994.1:c.*1192G>C ENSP00000496322.1:n.*1192G>C
ENST00000644037.1:c.*1402G>C ENSP00000496408.1:n.*1402G>C
ENST00000644055.1:c.*1817G>C ENSP00000496307.1:n.*1817G>C
ENST00000644126.1:n.2864G>C
ENST00000644217.1:c.1192G>C ENSP00000494646.1:p.Gly398Arg
ENST00000644265.1:c.561G>C
ENST00000644578.1:c.1006G>C ENSP00000495953.1:p.Gly336Arg
ENST00000644604.1:c.1192G>C ENSP00000495961.1:p.Gly398Arg
ENST00000644680.1:c.*1713G>C ENSP00000496173.1:n.*1713G>C
ENST00000644838.1:c.*575G>C ENSP00000495910.1:n.*575G>C
ENST00000644910.1:c.1799G>C
ENST00000645205.1:c.1192G>C ENSP00000495823.1:p.Gly398Arg
ENST00000645351.1:c.1192G>C ENSP00000494319.1:p.Gly398Arg
ENST00000645551.1:c.*909G>C ENSP00000495928.1:n.*909G>C
ENST00000645578.1:c.*966G>C ENSP00000496495.1:n.*966G>C
ENST00000645582.1:c.*1022G>C ENSP00000494980.1:n.*1022G>C
ENST00000645655.1:c.1192G>C ENSP00000495202.1:p.Gly398Arg
ENST00000645662.1:c.*651G>C ENSP00000495964.1:n.*651G>C
ENST00000645836.1:c.*966G>C ENSP00000493915.1:n.*966G>C
ENST00000645899.1:c.1192G>C ENSP00000496773.1:p.Gly398Arg
ENST00000645964.1:c.*1058G>C ENSP00000494208.1:n.*1058G>C
ENST00000646104.1:c.*1660G>C ENSP00000495475.1:n.*1660G>C
ENST00000646186.1:c.*864G>C ENSP00000493806.1:n.*864G>C
ENST00000646286.1:c.*1085G>C ENSP00000494291.1:n.*1085G>C
ENST00000646463.1:c.*957G>C ENSP00000494541.1:n.*957G>C
ENST00000646528.1:c.*1908G>C ENSP00000496553.1:n.*1908G>C
ENST00000646536.1:c.*482G>C ENSP00000494801.1:n.*482G>C
ENST00000646624.1:c.1192G>C ENSP00000494575.1:p.Gly398Arg
ENST00000646821.1:c.*482G>C ENSP00000495257.1:n.*482G>C
ENST00000646842.1:n.636G>C
ENST00000646848.1:c.*407G>C ENSP00000495831.1:n.*407G>C
ENST00000647186.1:c.1192G>C ENSP00000494775.1:p.Gly398Arg
ENST00000647233.1:n.2172G>C
ENST00000647322.1:c.783G>C
ENST00000647418.1:c.*966G>C ENSP00000493552.1:n.*966G>C
ENST00000647428.1:c.853G>C ENSP00000495630.1:p.Gly285Arg
ENST00000651186.1:c.853G>C ENSP00000498645.1:p.Gly285Arg
ENST00000366601.7:c.1192G>C ENSP00000355560.3:p.Gly398Arg
ENST00000406207.4:c.1192G>C ENSP00000384571.1:p.Gly398Arg
ENST00000472011.5:n.1244G>C
ENST00000543662.3:c.1345G>C ENSP00000439170.1:p.Gly449Arg
NM_001079515.2:c.1192G>C NP_001072983.1:p.Gly398Arg
NM_001287801.1:c.1345G>C NP_001274730.1:p.Gly449Arg
NM_001287802.1:c.853G>C NP_001274731.1:p.Gly285Arg
NM_003193.4:c.1192G>C NP_003184.1:p.Gly398Arg
NM_003193.5:c.1192G>C MANE Select NP_003184.1:p.Gly398Arg
NM_001079515.3:c.1192G>C NP_001072983.1:p.Gly398Arg
NM_001287801.2:c.1345G>C NP_001274730.1:p.Gly449Arg
NM_001287802.2:c.853G>C NP_001274731.1:p.Gly285Arg