Canonical Allele Identifier: CA344945037

Gene: TBCE

Linked Data

• MyVariant Identifiers: chr1:g.235602141G>T (hg19) ; chr1:g.235438826G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.235438826G>T , CM000663.2:g.235438826G>T	GRCh38
NC_000001.10:g.235602141G>T , CM000663.1:g.235602141G>T	GRCh37
NC_000001.9:g.233668764G>T	NCBI36
NG_009230.1:g.76414G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366601.8:c.985G>T	ENSP00000355560.4:p.Glu329Ter
ENST00000406207.5:c.1174G>T	ENSP00000384571.1:p.Glu392Ter
ENST00000472011.6:n.1898G>T
ENST00000543662.4:c.1327G>T	ENSP00000439170.1:p.Glu443Ter
ENST00000642339.1:c.*871G>T	ENSP00000495425.1:n.*871G>T
ENST00000642431.1:c.1751G>T
ENST00000642463.1:c.*1072G>T	ENSP00000495007.1:n.*1072G>T
ENST00000642503.1:c.*948G>T	ENSP00000494334.1:n.*948G>T
ENST00000642610.2:c.1174G>T MANE Select	ENSP00000494796.1:p.Glu392Ter
ENST00000642764.1:n.2005G>T
ENST00000643125.1:c.*189G>T	ENSP00000494102.1:n.*189G>T
ENST00000643142.1:c.*665G>T	ENSP00000494755.1:n.*665G>T
ENST00000643238.1:c.*194G>T	ENSP00000495916.1:n.*194G>T
ENST00000643410.1:c.*464G>T	ENSP00000495030.1:n.*464G>T
ENST00000643487.1:n.1861G>T
ENST00000643524.1:c.*759G>T	ENSP00000494026.1:n.*759G>T
ENST00000643615.1:c.*1116+1352G>T	ENSP00000496103.1:n.*1116+1352G>T
ENST00000643993.1:n.1310G>T
ENST00000643994.1:c.*1174G>T	ENSP00000496322.1:n.*1174G>T
ENST00000644037.1:c.*1384G>T	ENSP00000496408.1:n.*1384G>T
ENST00000644055.1:c.*1799G>T	ENSP00000496307.1:n.*1799G>T
ENST00000644126.1:n.2846G>T
ENST00000644217.1:c.1174G>T	ENSP00000494646.1:p.Glu392Ter
ENST00000644265.1:c.543G>T
ENST00000644578.1:c.988G>T	ENSP00000495953.1:p.Glu330Ter
ENST00000644604.1:c.1174G>T	ENSP00000495961.1:p.Glu392Ter
ENST00000644680.1:c.*1695G>T	ENSP00000496173.1:n.*1695G>T
ENST00000644838.1:c.*557G>T	ENSP00000495910.1:n.*557G>T
ENST00000644910.1:c.1781G>T
ENST00000645205.1:c.1174G>T	ENSP00000495823.1:p.Glu392Ter
ENST00000645351.1:c.1174G>T	ENSP00000494319.1:p.Glu392Ter
ENST00000645551.1:c.*891G>T	ENSP00000495928.1:n.*891G>T
ENST00000645578.1:c.*948G>T	ENSP00000496495.1:n.*948G>T
ENST00000645582.1:c.*1004G>T	ENSP00000494980.1:n.*1004G>T
ENST00000645655.1:c.1174G>T	ENSP00000495202.1:p.Glu392Ter
ENST00000645662.1:c.*633G>T	ENSP00000495964.1:n.*633G>T
ENST00000645836.1:c.*948G>T	ENSP00000493915.1:n.*948G>T
ENST00000645899.1:c.1174G>T	ENSP00000496773.1:p.Glu392Ter
ENST00000645964.1:c.*1040G>T	ENSP00000494208.1:n.*1040G>T
ENST00000646104.1:c.*1642G>T	ENSP00000495475.1:n.*1642G>T
ENST00000646186.1:c.*846G>T	ENSP00000493806.1:n.*846G>T
ENST00000646286.1:c.*1067G>T	ENSP00000494291.1:n.*1067G>T
ENST00000646463.1:c.*939G>T	ENSP00000494541.1:n.*939G>T
ENST00000646528.1:c.*1890G>T	ENSP00000496553.1:n.*1890G>T
ENST00000646536.1:c.*464G>T	ENSP00000494801.1:n.*464G>T
ENST00000646624.1:c.1174G>T	ENSP00000494575.1:p.Glu392Ter
ENST00000646821.1:c.*464G>T	ENSP00000495257.1:n.*464G>T
ENST00000646842.1:n.618G>T
ENST00000646848.1:c.*389G>T	ENSP00000495831.1:n.*389G>T
ENST00000647186.1:c.1174G>T	ENSP00000494775.1:p.Glu392Ter
ENST00000647233.1:n.2154G>T
ENST00000647322.1:c.765G>T
ENST00000647418.1:c.*948G>T	ENSP00000493552.1:n.*948G>T
ENST00000647428.1:c.835G>T	ENSP00000495630.1:p.Glu279Ter
ENST00000651186.1:c.835G>T	ENSP00000498645.1:p.Glu279Ter
ENST00000366601.7:c.1174G>T	ENSP00000355560.3:p.Glu392Ter
ENST00000406207.4:c.1174G>T	ENSP00000384571.1:p.Glu392Ter
ENST00000472011.5:n.1226G>T
ENST00000543662.3:c.1327G>T	ENSP00000439170.1:p.Glu443Ter
NM_001079515.2:c.1174G>T	NP_001072983.1:p.Glu392Ter
NM_001287801.1:c.1327G>T	NP_001274730.1:p.Glu443Ter
NM_001287802.1:c.835G>T	NP_001274731.1:p.Glu279Ter
NM_003193.4:c.1174G>T	NP_003184.1:p.Glu392Ter
NM_003193.5:c.1174G>T MANE Select	NP_003184.1:p.Glu392Ter
NM_001079515.3:c.1174G>T	NP_001072983.1:p.Glu392Ter
NM_001287801.2:c.1327G>T	NP_001274730.1:p.Glu443Ter
NM_001287802.2:c.835G>T	NP_001274731.1:p.Glu279Ter