Canonical Allele Identifier: CA344945949

Gene: TBCE

Linked Data

• MyVariant Identifiers: chr1:g.235602226T>C (hg19) ; chr1:g.235438911T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.235438911T>C , CM000663.2:g.235438911T>C	GRCh38
NC_000001.10:g.235602226T>C , CM000663.1:g.235602226T>C	GRCh37
NC_000001.9:g.233668849T>C	NCBI36
NG_009230.1:g.76499T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366601.8:c.1070T>C	ENSP00000355560.4:p.Phe357Ser
ENST00000406207.5:c.1259T>C	ENSP00000384571.1:p.Phe420Ser
ENST00000472011.6:n.1983T>C
ENST00000543662.4:c.1412T>C	ENSP00000439170.1:p.Phe471Ser
ENST00000642339.1:c.*956T>C	ENSP00000495425.1:n.*956T>C
ENST00000642431.1:c.1836T>C
ENST00000642463.1:c.*1157T>C	ENSP00000495007.1:n.*1157T>C
ENST00000642503.1:c.*1033T>C	ENSP00000494334.1:n.*1033T>C
ENST00000642610.2:c.1259T>C MANE Select	ENSP00000494796.1:p.Phe420Ser
ENST00000642764.1:n.2090T>C
ENST00000643125.1:c.*274T>C	ENSP00000494102.1:n.*274T>C
ENST00000643142.1:c.*750T>C	ENSP00000494755.1:n.*750T>C
ENST00000643238.1:c.*279T>C	ENSP00000495916.1:n.*279T>C
ENST00000643410.1:c.*549T>C	ENSP00000495030.1:n.*549T>C
ENST00000643487.1:n.1946T>C
ENST00000643524.1:c.*844T>C	ENSP00000494026.1:n.*844T>C
ENST00000643615.1:c.*1116+1437T>C	ENSP00000496103.1:n.*1116+1437T>C
ENST00000643993.1:n.1395T>C
ENST00000643994.1:c.*1259T>C	ENSP00000496322.1:n.*1259T>C
ENST00000644037.1:c.*1469T>C	ENSP00000496408.1:n.*1469T>C
ENST00000644055.1:c.*1884T>C	ENSP00000496307.1:n.*1884T>C
ENST00000644126.1:n.2931T>C
ENST00000644217.1:c.1259T>C	ENSP00000494646.1:p.Phe420Ser
ENST00000644265.1:c.628T>C
ENST00000644578.1:c.1073T>C	ENSP00000495953.1:p.Phe358Ser
ENST00000644604.1:c.1259T>C	ENSP00000495961.1:p.Phe420Ser
ENST00000644680.1:c.*1780T>C	ENSP00000496173.1:n.*1780T>C
ENST00000644838.1:c.*642T>C	ENSP00000495910.1:n.*642T>C
ENST00000644910.1:c.1866T>C
ENST00000645205.1:c.1259T>C	ENSP00000495823.1:p.Phe420Ser
ENST00000645351.1:c.1259T>C	ENSP00000494319.1:p.Phe420Ser
ENST00000645551.1:c.*976T>C	ENSP00000495928.1:n.*976T>C
ENST00000645578.1:c.*1033T>C	ENSP00000496495.1:n.*1033T>C
ENST00000645582.1:c.*1089T>C	ENSP00000494980.1:n.*1089T>C
ENST00000645655.1:c.1259T>C	ENSP00000495202.1:p.Phe420Ser
ENST00000645836.1:c.*1033T>C	ENSP00000493915.1:n.*1033T>C
ENST00000645899.1:c.1259T>C	ENSP00000496773.1:p.Phe420Ser
ENST00000645964.1:c.*1125T>C	ENSP00000494208.1:n.*1125T>C
ENST00000646104.1:c.*1727T>C	ENSP00000495475.1:n.*1727T>C
ENST00000646186.1:c.*931T>C	ENSP00000493806.1:n.*931T>C
ENST00000646286.1:c.*1152T>C	ENSP00000494291.1:n.*1152T>C
ENST00000646463.1:c.*1024T>C	ENSP00000494541.1:n.*1024T>C
ENST00000646528.1:c.*1975T>C	ENSP00000496553.1:n.*1975T>C
ENST00000646536.1:c.*549T>C	ENSP00000494801.1:n.*549T>C
ENST00000646624.1:c.1259T>C	ENSP00000494575.1:p.Phe420Ser
ENST00000646821.1:c.*549T>C	ENSP00000495257.1:n.*549T>C
ENST00000646842.1:n.703T>C
ENST00000646848.1:c.*474T>C	ENSP00000495831.1:n.*474T>C
ENST00000647186.1:c.1259T>C	ENSP00000494775.1:p.Phe420Ser
ENST00000647233.1:n.2239T>C
ENST00000647322.1:c.850T>C
ENST00000647418.1:c.*1033T>C	ENSP00000493552.1:n.*1033T>C
ENST00000647428.1:c.920T>C	ENSP00000495630.1:p.Phe307Ser
ENST00000651186.1:c.920T>C	ENSP00000498645.1:p.Phe307Ser
ENST00000366601.7:c.1259T>C	ENSP00000355560.3:p.Phe420Ser
ENST00000406207.4:c.1259T>C	ENSP00000384571.1:p.Phe420Ser
ENST00000472011.5:n.1311T>C
ENST00000543662.3:c.1412T>C	ENSP00000439170.1:p.Phe471Ser
NM_001079515.2:c.1259T>C	NP_001072983.1:p.Phe420Ser
NM_001287801.1:c.1412T>C	NP_001274730.1:p.Phe471Ser
NM_001287802.1:c.920T>C	NP_001274731.1:p.Phe307Ser
NM_003193.4:c.1259T>C	NP_003184.1:p.Phe420Ser
NM_003193.5:c.1259T>C MANE Select	NP_003184.1:p.Phe420Ser
NM_001079515.3:c.1259T>C	NP_001072983.1:p.Phe420Ser
NM_001287801.2:c.1412T>C	NP_001274730.1:p.Phe471Ser
NM_001287802.2:c.920T>C	NP_001274731.1:p.Phe307Ser