Canonical Allele Identifier: CA344944547

Gene: TBCE

Linked Data

• MyVariant Identifiers: chr1:g.235602085T>G (hg19) ; chr1:g.235438770T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.235438770T>G , CM000663.2:g.235438770T>G	GRCh38
NC_000001.10:g.235602085T>G , CM000663.1:g.235602085T>G	GRCh37
NC_000001.9:g.233668708T>G	NCBI36
NG_009230.1:g.76358T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366601.8:c.929T>G	ENSP00000355560.4:p.Ile310Ser
ENST00000406207.5:c.1118T>G	ENSP00000384571.1:p.Ile373Ser
ENST00000472011.6:n.1842T>G
ENST00000543662.4:c.1271T>G	ENSP00000439170.1:p.Ile424Ser
ENST00000642339.1:c.*815T>G	ENSP00000495425.1:n.*815T>G
ENST00000642431.1:c.1695T>G
ENST00000642463.1:c.*1016T>G	ENSP00000495007.1:n.*1016T>G
ENST00000642503.1:c.*892T>G	ENSP00000494334.1:n.*892T>G
ENST00000642610.2:c.1118T>G MANE Select	ENSP00000494796.1:p.Ile373Ser
ENST00000642764.1:n.1949T>G
ENST00000643125.1:c.*133T>G	ENSP00000494102.1:n.*133T>G
ENST00000643142.1:c.*609T>G	ENSP00000494755.1:n.*609T>G
ENST00000643238.1:c.*138T>G	ENSP00000495916.1:n.*138T>G
ENST00000643410.1:c.*408T>G	ENSP00000495030.1:n.*408T>G
ENST00000643487.1:n.1805T>G
ENST00000643524.1:c.*703T>G	ENSP00000494026.1:n.*703T>G
ENST00000643615.1:c.*1116+1296T>G	ENSP00000496103.1:n.*1116+1296T>G
ENST00000643993.1:n.1254T>G
ENST00000643994.1:c.*1118T>G	ENSP00000496322.1:n.*1118T>G
ENST00000644037.1:c.*1328T>G	ENSP00000496408.1:n.*1328T>G
ENST00000644055.1:c.*1743T>G	ENSP00000496307.1:n.*1743T>G
ENST00000644126.1:n.2790T>G
ENST00000644217.1:c.1118T>G	ENSP00000494646.1:p.Ile373Ser
ENST00000644265.1:c.487T>G
ENST00000644578.1:c.932T>G	ENSP00000495953.1:p.Ile311Ser
ENST00000644604.1:c.1118T>G	ENSP00000495961.1:p.Ile373Ser
ENST00000644680.1:c.*1639T>G	ENSP00000496173.1:n.*1639T>G
ENST00000644838.1:c.*501T>G	ENSP00000495910.1:n.*501T>G
ENST00000644910.1:c.1725T>G
ENST00000645205.1:c.1118T>G	ENSP00000495823.1:p.Ile373Ser
ENST00000645351.1:c.1118T>G	ENSP00000494319.1:p.Ile373Ser
ENST00000645551.1:c.*835T>G	ENSP00000495928.1:n.*835T>G
ENST00000645578.1:c.*892T>G	ENSP00000496495.1:n.*892T>G
ENST00000645582.1:c.*948T>G	ENSP00000494980.1:n.*948T>G
ENST00000645655.1:c.1118T>G	ENSP00000495202.1:p.Ile373Ser
ENST00000645662.1:c.*577T>G	ENSP00000495964.1:n.*577T>G
ENST00000645836.1:c.*892T>G	ENSP00000493915.1:n.*892T>G
ENST00000645899.1:c.1118T>G	ENSP00000496773.1:p.Ile373Ser
ENST00000645964.1:c.*984T>G	ENSP00000494208.1:n.*984T>G
ENST00000646104.1:c.*1586T>G	ENSP00000495475.1:n.*1586T>G
ENST00000646186.1:c.*790T>G	ENSP00000493806.1:n.*790T>G
ENST00000646286.1:c.*1011T>G	ENSP00000494291.1:n.*1011T>G
ENST00000646463.1:c.*883T>G	ENSP00000494541.1:n.*883T>G
ENST00000646528.1:c.*1834T>G	ENSP00000496553.1:n.*1834T>G
ENST00000646536.1:c.*408T>G	ENSP00000494801.1:n.*408T>G
ENST00000646624.1:c.1118T>G	ENSP00000494575.1:p.Ile373Ser
ENST00000646821.1:c.*408T>G	ENSP00000495257.1:n.*408T>G
ENST00000646842.1:n.562T>G
ENST00000646848.1:c.*333T>G	ENSP00000495831.1:n.*333T>G
ENST00000647186.1:c.1118T>G	ENSP00000494775.1:p.Ile373Ser
ENST00000647233.1:n.2098T>G
ENST00000647322.1:c.709T>G
ENST00000647418.1:c.*892T>G	ENSP00000493552.1:n.*892T>G
ENST00000647428.1:c.779T>G	ENSP00000495630.1:p.Ile260Ser
ENST00000651186.1:c.779T>G	ENSP00000498645.1:p.Ile260Ser
ENST00000366601.7:c.1118T>G	ENSP00000355560.3:p.Ile373Ser
ENST00000406207.4:c.1118T>G	ENSP00000384571.1:p.Ile373Ser
ENST00000472011.5:n.1170T>G
ENST00000543662.3:c.1271T>G	ENSP00000439170.1:p.Ile424Ser
NM_001079515.2:c.1118T>G	NP_001072983.1:p.Ile373Ser
NM_001287801.1:c.1271T>G	NP_001274730.1:p.Ile424Ser
NM_001287802.1:c.779T>G	NP_001274731.1:p.Ile260Ser
NM_003193.4:c.1118T>G	NP_003184.1:p.Ile373Ser
NM_003193.5:c.1118T>G MANE Select	NP_003184.1:p.Ile373Ser
NM_001079515.3:c.1118T>G	NP_001072983.1:p.Ile373Ser
NM_001287801.2:c.1271T>G	NP_001274730.1:p.Ile424Ser
NM_001287802.2:c.779T>G	NP_001274731.1:p.Ile260Ser