Canonical Allele Identifier: CA344942263

Gene: TBCE

Linked Data

• MyVariant Identifiers: chr1:g.235600706A>T (hg19) ; chr1:g.235437391A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.235437391A>T , CM000663.2:g.235437391A>T	GRCh38
NC_000001.10:g.235600706A>T , CM000663.1:g.235600706A>T	GRCh37
NC_000001.9:g.233667329A>T	NCBI36
NG_009230.1:g.74979A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366601.8:c.844A>T	ENSP00000355560.4:p.Thr282Ser
ENST00000406207.5:c.1033A>T	ENSP00000384571.1:p.Thr345Ser
ENST00000472011.6:n.1757A>T
ENST00000543662.4:c.1186A>T	ENSP00000439170.1:p.Thr396Ser
ENST00000642339.1:c.*730A>T	ENSP00000495425.1:n.*730A>T
ENST00000642431.1:c.1610A>T
ENST00000642463.1:c.*931A>T	ENSP00000495007.1:n.*931A>T
ENST00000642503.1:c.*807A>T	ENSP00000494334.1:n.*807A>T
ENST00000642610.2:c.1033A>T MANE Select	ENSP00000494796.1:p.Thr345Ser
ENST00000642764.1:n.1864A>T
ENST00000643125.1:c.*48A>T	ENSP00000494102.1:n.*48A>T
ENST00000643142.1:c.*524A>T	ENSP00000494755.1:n.*524A>T
ENST00000643238.1:c.*53A>T	ENSP00000495916.1:n.*53A>T
ENST00000643410.1:c.*323A>T	ENSP00000495030.1:n.*323A>T
ENST00000643487.1:n.1720A>T
ENST00000643524.1:c.*618A>T	ENSP00000494026.1:n.*618A>T
ENST00000643615.1:c.*1033A>T	ENSP00000496103.1:n.*1033A>T
ENST00000643993.1:n.1169A>T
ENST00000643994.1:c.*1033A>T	ENSP00000496322.1:n.*1033A>T
ENST00000644037.1:c.*1243A>T	ENSP00000496408.1:n.*1243A>T
ENST00000644055.1:c.*1658A>T	ENSP00000496307.1:n.*1658A>T
ENST00000644126.1:n.2705A>T
ENST00000644217.1:c.1033A>T	ENSP00000494646.1:p.Thr345Ser
ENST00000644265.1:c.402A>T
ENST00000644578.1:c.847A>T	ENSP00000495953.1:p.Thr283Ser
ENST00000644604.1:c.1033A>T	ENSP00000495961.1:p.Thr345Ser
ENST00000644680.1:c.*1554A>T	ENSP00000496173.1:n.*1554A>T
ENST00000644838.1:c.*416A>T	ENSP00000495910.1:n.*416A>T
ENST00000644910.1:c.1640A>T
ENST00000645205.1:c.1033A>T	ENSP00000495823.1:p.Thr345Ser
ENST00000645351.1:c.1033A>T	ENSP00000494319.1:p.Thr345Ser
ENST00000645551.1:c.*750A>T	ENSP00000495928.1:n.*750A>T
ENST00000645578.1:c.*807A>T	ENSP00000496495.1:n.*807A>T
ENST00000645582.1:c.*863A>T	ENSP00000494980.1:n.*863A>T
ENST00000645655.1:c.1033A>T	ENSP00000495202.1:p.Thr345Ser
ENST00000645662.1:c.*492A>T	ENSP00000495964.1:n.*492A>T
ENST00000645836.1:c.*807A>T	ENSP00000493915.1:n.*807A>T
ENST00000645899.1:c.1033A>T	ENSP00000496773.1:p.Thr345Ser
ENST00000645964.1:c.*899A>T	ENSP00000494208.1:n.*899A>T
ENST00000646104.1:c.*1501A>T	ENSP00000495475.1:n.*1501A>T
ENST00000646186.1:c.*705A>T	ENSP00000493806.1:n.*705A>T
ENST00000646281.1:c.1033A>T	ENSP00000495225.1:p.Thr345Ser
ENST00000646286.1:c.*926A>T	ENSP00000494291.1:n.*926A>T
ENST00000646463.1:c.*798A>T	ENSP00000494541.1:n.*798A>T
ENST00000646528.1:c.*1749A>T	ENSP00000496553.1:n.*1749A>T
ENST00000646536.1:c.*323A>T	ENSP00000494801.1:n.*323A>T
ENST00000646624.1:c.1033A>T	ENSP00000494575.1:p.Thr345Ser
ENST00000646821.1:c.*323A>T	ENSP00000495257.1:n.*323A>T
ENST00000646842.1:n.477A>T
ENST00000646848.1:c.*248A>T	ENSP00000495831.1:n.*248A>T
ENST00000647186.1:c.1033A>T	ENSP00000494775.1:p.Thr345Ser
ENST00000647233.1:n.2013A>T
ENST00000647322.1:c.624A>T
ENST00000647418.1:c.*807A>T	ENSP00000493552.1:n.*807A>T
ENST00000647428.1:c.694A>T	ENSP00000495630.1:p.Thr232Ser
ENST00000651186.1:c.694A>T	ENSP00000498645.1:p.Thr232Ser
ENST00000366601.7:c.1033A>T	ENSP00000355560.3:p.Thr345Ser
ENST00000406207.4:c.1033A>T	ENSP00000384571.1:p.Thr345Ser
ENST00000472011.5:n.1085A>T
ENST00000543662.3:c.1186A>T	ENSP00000439170.1:p.Thr396Ser
NM_001079515.2:c.1033A>T	NP_001072983.1:p.Thr345Ser
NM_001287801.1:c.1186A>T	NP_001274730.1:p.Thr396Ser
NM_001287802.1:c.694A>T	NP_001274731.1:p.Thr232Ser
NM_003193.4:c.1033A>T	NP_003184.1:p.Thr345Ser
NM_003193.5:c.1033A>T MANE Select	NP_003184.1:p.Thr345Ser
NM_001079515.3:c.1033A>T	NP_001072983.1:p.Thr345Ser
NM_001287801.2:c.1186A>T	NP_001274730.1:p.Thr396Ser
NM_001287802.2:c.694A>T	NP_001274731.1:p.Thr232Ser