Canonical Allele Identifier: CA2486499888
Gene: TBCE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.235438841G= , CM000663.2:g.235438841G= GRCh38
NC_000001.10:g.235602156G= , CM000663.1:g.235602156G= GRCh37
NC_000001.9:g.233668779G= NCBI36
NG_009230.1:g.76429G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000366601.8:c.1000G= ENSP00000355560.4:p.Gly334=
ENST00000406207.5:c.1189G= ENSP00000384571.1:p.Gly397=
ENST00000472011.6:n.1913G=
ENST00000543662.4:c.1342G= ENSP00000439170.1:p.Gly448=
ENST00000642339.1:c.*886G= ENSP00000495425.1:n.*886G=
ENST00000642431.1:c.1766G=
ENST00000642463.1:c.*1087G= ENSP00000495007.1:n.*1087G=
ENST00000642503.1:c.*963G= ENSP00000494334.1:n.*963G=
ENST00000642610.2:c.1189G= MANE Select ENSP00000494796.1:p.Gly397=
ENST00000642764.1:n.2020G=
ENST00000643125.1:c.*204G= ENSP00000494102.1:n.*204G=
ENST00000643142.1:c.*680G= ENSP00000494755.1:n.*680G=
ENST00000643238.1:c.*209G= ENSP00000495916.1:n.*209G=
ENST00000643410.1:c.*479G= ENSP00000495030.1:n.*479G=
ENST00000643487.1:n.1876G=
ENST00000643524.1:c.*774G= ENSP00000494026.1:n.*774G=
ENST00000643615.1:c.*1116+1367G= ENSP00000496103.1:n.*1116+1367G=
ENST00000643993.1:n.1325G=
ENST00000643994.1:c.*1189G= ENSP00000496322.1:n.*1189G=
ENST00000644037.1:c.*1399G= ENSP00000496408.1:n.*1399G=
ENST00000644055.1:c.*1814G= ENSP00000496307.1:n.*1814G=
ENST00000644126.1:n.2861G=
ENST00000644217.1:c.1189G= ENSP00000494646.1:p.Gly397=
ENST00000644265.1:c.558G=
ENST00000644578.1:c.1003G= ENSP00000495953.1:p.Gly335=
ENST00000644604.1:c.1189G= ENSP00000495961.1:p.Gly397=
ENST00000644680.1:c.*1710G= ENSP00000496173.1:n.*1710G=
ENST00000644838.1:c.*572G= ENSP00000495910.1:n.*572G=
ENST00000644910.1:c.1796G=
ENST00000645205.1:c.1189G= ENSP00000495823.1:p.Gly397=
ENST00000645351.1:c.1189G= ENSP00000494319.1:p.Gly397=
ENST00000645551.1:c.*906G= ENSP00000495928.1:n.*906G=
ENST00000645578.1:c.*963G= ENSP00000496495.1:n.*963G=
ENST00000645582.1:c.*1019G= ENSP00000494980.1:n.*1019G=
ENST00000645655.1:c.1189G= ENSP00000495202.1:p.Gly397=
ENST00000645662.1:c.*648G= ENSP00000495964.1:n.*648G=
ENST00000645836.1:c.*963G= ENSP00000493915.1:n.*963G=
ENST00000645899.1:c.1189G= ENSP00000496773.1:p.Gly397=
ENST00000645964.1:c.*1055G= ENSP00000494208.1:n.*1055G=
ENST00000646104.1:c.*1657G= ENSP00000495475.1:n.*1657G=
ENST00000646186.1:c.*861G= ENSP00000493806.1:n.*861G=
ENST00000646286.1:c.*1082G= ENSP00000494291.1:n.*1082G=
ENST00000646463.1:c.*954G= ENSP00000494541.1:n.*954G=
ENST00000646528.1:c.*1905G= ENSP00000496553.1:n.*1905G=
ENST00000646536.1:c.*479G= ENSP00000494801.1:n.*479G=
ENST00000646624.1:c.1189G= ENSP00000494575.1:p.Gly397=
ENST00000646821.1:c.*479G= ENSP00000495257.1:n.*479G=
ENST00000646842.1:n.633G=
ENST00000646848.1:c.*404G= ENSP00000495831.1:n.*404G=
ENST00000647186.1:c.1189G= ENSP00000494775.1:p.Gly397=
ENST00000647233.1:n.2169G=
ENST00000647322.1:c.780G=
ENST00000647418.1:c.*963G= ENSP00000493552.1:n.*963G=
ENST00000647428.1:c.850G= ENSP00000495630.1:p.Gly284=
ENST00000651186.1:c.850G= ENSP00000498645.1:p.Gly284=
ENST00000366601.7:c.1189G= ENSP00000355560.3:p.Gly397=
ENST00000406207.4:c.1189G= ENSP00000384571.1:p.Gly397=
ENST00000472011.5:n.1241G=
ENST00000543662.3:c.1342G= ENSP00000439170.1:p.Gly448=
NM_001079515.2:c.1189G= NP_001072983.1:p.Gly397=
NM_001287801.1:c.1342G= NP_001274730.1:p.Gly448=
NM_001287802.1:c.850G= NP_001274731.1:p.Gly284=
NM_003193.4:c.1189G= NP_003184.1:p.Gly397=
NM_003193.5:c.1189G= MANE Select NP_003184.1:p.Gly397=
NM_001079515.3:c.1189G= NP_001072983.1:p.Gly397=
NM_001287801.2:c.1342G= NP_001274730.1:p.Gly448=
NM_001287802.2:c.850G= NP_001274731.1:p.Gly284=