Canonical Allele Identifier: CA344945406

Gene: TBCE

Linked Data

• MyVariant Identifiers: chr1:g.235602178A>G (hg19) ; chr1:g.235438863A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.235438863A>G , CM000663.2:g.235438863A>G	GRCh38
NC_000001.10:g.235602178A>G , CM000663.1:g.235602178A>G	GRCh37
NC_000001.9:g.233668801A>G	NCBI36
NG_009230.1:g.76451A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366601.8:c.1022A>G	ENSP00000355560.4:p.Lys341Arg
ENST00000406207.5:c.1211A>G	ENSP00000384571.1:p.Lys404Arg
ENST00000472011.6:n.1935A>G
ENST00000543662.4:c.1364A>G	ENSP00000439170.1:p.Lys455Arg
ENST00000642339.1:c.*908A>G	ENSP00000495425.1:n.*908A>G
ENST00000642431.1:c.1788A>G
ENST00000642463.1:c.*1109A>G	ENSP00000495007.1:n.*1109A>G
ENST00000642503.1:c.*985A>G	ENSP00000494334.1:n.*985A>G
ENST00000642610.2:c.1211A>G MANE Select	ENSP00000494796.1:p.Lys404Arg
ENST00000642764.1:n.2042A>G
ENST00000643125.1:c.*226A>G	ENSP00000494102.1:n.*226A>G
ENST00000643142.1:c.*702A>G	ENSP00000494755.1:n.*702A>G
ENST00000643238.1:c.*231A>G	ENSP00000495916.1:n.*231A>G
ENST00000643410.1:c.*501A>G	ENSP00000495030.1:n.*501A>G
ENST00000643487.1:n.1898A>G
ENST00000643524.1:c.*796A>G	ENSP00000494026.1:n.*796A>G
ENST00000643615.1:c.*1116+1389A>G	ENSP00000496103.1:n.*1116+1389A>G
ENST00000643993.1:n.1347A>G
ENST00000643994.1:c.*1211A>G	ENSP00000496322.1:n.*1211A>G
ENST00000644037.1:c.*1421A>G	ENSP00000496408.1:n.*1421A>G
ENST00000644055.1:c.*1836A>G	ENSP00000496307.1:n.*1836A>G
ENST00000644126.1:n.2883A>G
ENST00000644217.1:c.1211A>G	ENSP00000494646.1:p.Lys404Arg
ENST00000644265.1:c.580A>G
ENST00000644578.1:c.1025A>G	ENSP00000495953.1:p.Lys342Arg
ENST00000644604.1:c.1211A>G	ENSP00000495961.1:p.Lys404Arg
ENST00000644680.1:c.*1732A>G	ENSP00000496173.1:n.*1732A>G
ENST00000644838.1:c.*594A>G	ENSP00000495910.1:n.*594A>G
ENST00000644910.1:c.1818A>G
ENST00000645205.1:c.1211A>G	ENSP00000495823.1:p.Lys404Arg
ENST00000645351.1:c.1211A>G	ENSP00000494319.1:p.Lys404Arg
ENST00000645551.1:c.*928A>G	ENSP00000495928.1:n.*928A>G
ENST00000645578.1:c.*985A>G	ENSP00000496495.1:n.*985A>G
ENST00000645582.1:c.*1041A>G	ENSP00000494980.1:n.*1041A>G
ENST00000645655.1:c.1211A>G	ENSP00000495202.1:p.Lys404Arg
ENST00000645662.1:c.*670A>G	ENSP00000495964.1:n.*670A>G
ENST00000645836.1:c.*985A>G	ENSP00000493915.1:n.*985A>G
ENST00000645899.1:c.1211A>G	ENSP00000496773.1:p.Lys404Arg
ENST00000645964.1:c.*1077A>G	ENSP00000494208.1:n.*1077A>G
ENST00000646104.1:c.*1679A>G	ENSP00000495475.1:n.*1679A>G
ENST00000646186.1:c.*883A>G	ENSP00000493806.1:n.*883A>G
ENST00000646286.1:c.*1104A>G	ENSP00000494291.1:n.*1104A>G
ENST00000646463.1:c.*976A>G	ENSP00000494541.1:n.*976A>G
ENST00000646528.1:c.*1927A>G	ENSP00000496553.1:n.*1927A>G
ENST00000646536.1:c.*501A>G	ENSP00000494801.1:n.*501A>G
ENST00000646624.1:c.1211A>G	ENSP00000494575.1:p.Lys404Arg
ENST00000646821.1:c.*501A>G	ENSP00000495257.1:n.*501A>G
ENST00000646842.1:n.655A>G
ENST00000646848.1:c.*426A>G	ENSP00000495831.1:n.*426A>G
ENST00000647186.1:c.1211A>G	ENSP00000494775.1:p.Lys404Arg
ENST00000647233.1:n.2191A>G
ENST00000647322.1:c.802A>G
ENST00000647418.1:c.*985A>G	ENSP00000493552.1:n.*985A>G
ENST00000647428.1:c.872A>G	ENSP00000495630.1:p.Lys291Arg
ENST00000651186.1:c.872A>G	ENSP00000498645.1:p.Lys291Arg
ENST00000366601.7:c.1211A>G	ENSP00000355560.3:p.Lys404Arg
ENST00000406207.4:c.1211A>G	ENSP00000384571.1:p.Lys404Arg
ENST00000472011.5:n.1263A>G
ENST00000543662.3:c.1364A>G	ENSP00000439170.1:p.Lys455Arg
NM_001079515.2:c.1211A>G	NP_001072983.1:p.Lys404Arg
NM_001287801.1:c.1364A>G	NP_001274730.1:p.Lys455Arg
NM_001287802.1:c.872A>G	NP_001274731.1:p.Lys291Arg
NM_003193.4:c.1211A>G	NP_003184.1:p.Lys404Arg
NM_003193.5:c.1211A>G MANE Select	NP_003184.1:p.Lys404Arg
NM_001079515.3:c.1211A>G	NP_001072983.1:p.Lys404Arg
NM_001287801.2:c.1364A>G	NP_001274730.1:p.Lys455Arg
NM_001287802.2:c.872A>G	NP_001274731.1:p.Lys291Arg