Canonical Allele Identifier: CA344945339

Gene: TBCE

Linked Data

• MyVariant Identifiers: chr1:g.235602171C>A (hg19) ; chr1:g.235438856C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.235438856C>A , CM000663.2:g.235438856C>A	GRCh38
NC_000001.10:g.235602171C>A , CM000663.1:g.235602171C>A	GRCh37
NC_000001.9:g.233668794C>A	NCBI36
NG_009230.1:g.76444C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366601.8:c.1015C>A	ENSP00000355560.4:p.Pro339Thr
ENST00000406207.5:c.1204C>A	ENSP00000384571.1:p.Pro402Thr
ENST00000472011.6:n.1928C>A
ENST00000543662.4:c.1357C>A	ENSP00000439170.1:p.Pro453Thr
ENST00000642339.1:c.*901C>A	ENSP00000495425.1:n.*901C>A
ENST00000642431.1:c.1781C>A
ENST00000642463.1:c.*1102C>A	ENSP00000495007.1:n.*1102C>A
ENST00000642503.1:c.*978C>A	ENSP00000494334.1:n.*978C>A
ENST00000642610.2:c.1204C>A MANE Select	ENSP00000494796.1:p.Pro402Thr
ENST00000642764.1:n.2035C>A
ENST00000643125.1:c.*219C>A	ENSP00000494102.1:n.*219C>A
ENST00000643142.1:c.*695C>A	ENSP00000494755.1:n.*695C>A
ENST00000643238.1:c.*224C>A	ENSP00000495916.1:n.*224C>A
ENST00000643410.1:c.*494C>A	ENSP00000495030.1:n.*494C>A
ENST00000643487.1:n.1891C>A
ENST00000643524.1:c.*789C>A	ENSP00000494026.1:n.*789C>A
ENST00000643615.1:c.*1116+1382C>A	ENSP00000496103.1:n.*1116+1382C>A
ENST00000643993.1:n.1340C>A
ENST00000643994.1:c.*1204C>A	ENSP00000496322.1:n.*1204C>A
ENST00000644037.1:c.*1414C>A	ENSP00000496408.1:n.*1414C>A
ENST00000644055.1:c.*1829C>A	ENSP00000496307.1:n.*1829C>A
ENST00000644126.1:n.2876C>A
ENST00000644217.1:c.1204C>A	ENSP00000494646.1:p.Pro402Thr
ENST00000644265.1:c.573C>A
ENST00000644578.1:c.1018C>A	ENSP00000495953.1:p.Pro340Thr
ENST00000644604.1:c.1204C>A	ENSP00000495961.1:p.Pro402Thr
ENST00000644680.1:c.*1725C>A	ENSP00000496173.1:n.*1725C>A
ENST00000644838.1:c.*587C>A	ENSP00000495910.1:n.*587C>A
ENST00000644910.1:c.1811C>A
ENST00000645205.1:c.1204C>A	ENSP00000495823.1:p.Pro402Thr
ENST00000645351.1:c.1204C>A	ENSP00000494319.1:p.Pro402Thr
ENST00000645551.1:c.*921C>A	ENSP00000495928.1:n.*921C>A
ENST00000645578.1:c.*978C>A	ENSP00000496495.1:n.*978C>A
ENST00000645582.1:c.*1034C>A	ENSP00000494980.1:n.*1034C>A
ENST00000645655.1:c.1204C>A	ENSP00000495202.1:p.Pro402Thr
ENST00000645662.1:c.*663C>A	ENSP00000495964.1:n.*663C>A
ENST00000645836.1:c.*978C>A	ENSP00000493915.1:n.*978C>A
ENST00000645899.1:c.1204C>A	ENSP00000496773.1:p.Pro402Thr
ENST00000645964.1:c.*1070C>A	ENSP00000494208.1:n.*1070C>A
ENST00000646104.1:c.*1672C>A	ENSP00000495475.1:n.*1672C>A
ENST00000646186.1:c.*876C>A	ENSP00000493806.1:n.*876C>A
ENST00000646286.1:c.*1097C>A	ENSP00000494291.1:n.*1097C>A
ENST00000646463.1:c.*969C>A	ENSP00000494541.1:n.*969C>A
ENST00000646528.1:c.*1920C>A	ENSP00000496553.1:n.*1920C>A
ENST00000646536.1:c.*494C>A	ENSP00000494801.1:n.*494C>A
ENST00000646624.1:c.1204C>A	ENSP00000494575.1:p.Pro402Thr
ENST00000646821.1:c.*494C>A	ENSP00000495257.1:n.*494C>A
ENST00000646842.1:n.648C>A
ENST00000646848.1:c.*419C>A	ENSP00000495831.1:n.*419C>A
ENST00000647186.1:c.1204C>A	ENSP00000494775.1:p.Pro402Thr
ENST00000647233.1:n.2184C>A
ENST00000647322.1:c.795C>A
ENST00000647418.1:c.*978C>A	ENSP00000493552.1:n.*978C>A
ENST00000647428.1:c.865C>A	ENSP00000495630.1:p.Pro289Thr
ENST00000651186.1:c.865C>A	ENSP00000498645.1:p.Pro289Thr
ENST00000366601.7:c.1204C>A	ENSP00000355560.3:p.Pro402Thr
ENST00000406207.4:c.1204C>A	ENSP00000384571.1:p.Pro402Thr
ENST00000472011.5:n.1256C>A
ENST00000543662.3:c.1357C>A	ENSP00000439170.1:p.Pro453Thr
NM_001079515.2:c.1204C>A	NP_001072983.1:p.Pro402Thr
NM_001287801.1:c.1357C>A	NP_001274730.1:p.Pro453Thr
NM_001287802.1:c.865C>A	NP_001274731.1:p.Pro289Thr
NM_003193.4:c.1204C>A	NP_003184.1:p.Pro402Thr
NM_003193.5:c.1204C>A MANE Select	NP_003184.1:p.Pro402Thr
NM_001079515.3:c.1204C>A	NP_001072983.1:p.Pro402Thr
NM_001287801.2:c.1357C>A	NP_001274730.1:p.Pro453Thr
NM_001287802.2:c.865C>A	NP_001274731.1:p.Pro289Thr