Canonical Allele Identifier: CA344945269

Gene: TBCE

Linked Data

• MyVariant Identifiers: chr1:g.235602162C>G (hg19) ; chr1:g.235438847C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.235438847C>G , CM000663.2:g.235438847C>G	GRCh38
NC_000001.10:g.235602162C>G , CM000663.1:g.235602162C>G	GRCh37
NC_000001.9:g.233668785C>G	NCBI36
NG_009230.1:g.76435C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366601.8:c.1006C>G	ENSP00000355560.4:p.His336Asp
ENST00000406207.5:c.1195C>G	ENSP00000384571.1:p.His399Asp
ENST00000472011.6:n.1919C>G
ENST00000543662.4:c.1348C>G	ENSP00000439170.1:p.His450Asp
ENST00000642339.1:c.*892C>G	ENSP00000495425.1:n.*892C>G
ENST00000642431.1:c.1772C>G
ENST00000642463.1:c.*1093C>G	ENSP00000495007.1:n.*1093C>G
ENST00000642503.1:c.*969C>G	ENSP00000494334.1:n.*969C>G
ENST00000642610.2:c.1195C>G MANE Select	ENSP00000494796.1:p.His399Asp
ENST00000642764.1:n.2026C>G
ENST00000643125.1:c.*210C>G	ENSP00000494102.1:n.*210C>G
ENST00000643142.1:c.*686C>G	ENSP00000494755.1:n.*686C>G
ENST00000643238.1:c.*215C>G	ENSP00000495916.1:n.*215C>G
ENST00000643410.1:c.*485C>G	ENSP00000495030.1:n.*485C>G
ENST00000643487.1:n.1882C>G
ENST00000643524.1:c.*780C>G	ENSP00000494026.1:n.*780C>G
ENST00000643615.1:c.*1116+1373C>G	ENSP00000496103.1:n.*1116+1373C>G
ENST00000643993.1:n.1331C>G
ENST00000643994.1:c.*1195C>G	ENSP00000496322.1:n.*1195C>G
ENST00000644037.1:c.*1405C>G	ENSP00000496408.1:n.*1405C>G
ENST00000644055.1:c.*1820C>G	ENSP00000496307.1:n.*1820C>G
ENST00000644126.1:n.2867C>G
ENST00000644217.1:c.1195C>G	ENSP00000494646.1:p.His399Asp
ENST00000644265.1:c.564C>G
ENST00000644578.1:c.1009C>G	ENSP00000495953.1:p.His337Asp
ENST00000644604.1:c.1195C>G	ENSP00000495961.1:p.His399Asp
ENST00000644680.1:c.*1716C>G	ENSP00000496173.1:n.*1716C>G
ENST00000644838.1:c.*578C>G	ENSP00000495910.1:n.*578C>G
ENST00000644910.1:c.1802C>G
ENST00000645205.1:c.1195C>G	ENSP00000495823.1:p.His399Asp
ENST00000645351.1:c.1195C>G	ENSP00000494319.1:p.His399Asp
ENST00000645551.1:c.*912C>G	ENSP00000495928.1:n.*912C>G
ENST00000645578.1:c.*969C>G	ENSP00000496495.1:n.*969C>G
ENST00000645582.1:c.*1025C>G	ENSP00000494980.1:n.*1025C>G
ENST00000645655.1:c.1195C>G	ENSP00000495202.1:p.His399Asp
ENST00000645662.1:c.*654C>G	ENSP00000495964.1:n.*654C>G
ENST00000645836.1:c.*969C>G	ENSP00000493915.1:n.*969C>G
ENST00000645899.1:c.1195C>G	ENSP00000496773.1:p.His399Asp
ENST00000645964.1:c.*1061C>G	ENSP00000494208.1:n.*1061C>G
ENST00000646104.1:c.*1663C>G	ENSP00000495475.1:n.*1663C>G
ENST00000646186.1:c.*867C>G	ENSP00000493806.1:n.*867C>G
ENST00000646286.1:c.*1088C>G	ENSP00000494291.1:n.*1088C>G
ENST00000646463.1:c.*960C>G	ENSP00000494541.1:n.*960C>G
ENST00000646528.1:c.*1911C>G	ENSP00000496553.1:n.*1911C>G
ENST00000646536.1:c.*485C>G	ENSP00000494801.1:n.*485C>G
ENST00000646624.1:c.1195C>G	ENSP00000494575.1:p.His399Asp
ENST00000646821.1:c.*485C>G	ENSP00000495257.1:n.*485C>G
ENST00000646842.1:n.639C>G
ENST00000646848.1:c.*410C>G	ENSP00000495831.1:n.*410C>G
ENST00000647186.1:c.1195C>G	ENSP00000494775.1:p.His399Asp
ENST00000647233.1:n.2175C>G
ENST00000647322.1:c.786C>G
ENST00000647418.1:c.*969C>G	ENSP00000493552.1:n.*969C>G
ENST00000647428.1:c.856C>G	ENSP00000495630.1:p.His286Asp
ENST00000651186.1:c.856C>G	ENSP00000498645.1:p.His286Asp
ENST00000366601.7:c.1195C>G	ENSP00000355560.3:p.His399Asp
ENST00000406207.4:c.1195C>G	ENSP00000384571.1:p.His399Asp
ENST00000472011.5:n.1247C>G
ENST00000543662.3:c.1348C>G	ENSP00000439170.1:p.His450Asp
NM_001079515.2:c.1195C>G	NP_001072983.1:p.His399Asp
NM_001287801.1:c.1348C>G	NP_001274730.1:p.His450Asp
NM_001287802.1:c.856C>G	NP_001274731.1:p.His286Asp
NM_003193.4:c.1195C>G	NP_003184.1:p.His399Asp
NM_003193.5:c.1195C>G MANE Select	NP_003184.1:p.His399Asp
NM_001079515.3:c.1195C>G	NP_001072983.1:p.His399Asp
NM_001287801.2:c.1348C>G	NP_001274730.1:p.His450Asp
NM_001287802.2:c.856C>G	NP_001274731.1:p.His286Asp