Canonical Allele Identifier: CA344944677

Gene: TBCE

Linked Data

• MyVariant Identifiers: chr1:g.235602101G>C (hg19) ; chr1:g.235438786G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.235438786G>C , CM000663.2:g.235438786G>C	GRCh38
NC_000001.10:g.235602101G>C , CM000663.1:g.235602101G>C	GRCh37
NC_000001.9:g.233668724G>C	NCBI36
NG_009230.1:g.76374G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366601.8:c.945G>C	ENSP00000355560.4:p.Arg315Ser
ENST00000406207.5:c.1134G>C	ENSP00000384571.1:p.Arg378Ser
ENST00000472011.6:n.1858G>C
ENST00000543662.4:c.1287G>C	ENSP00000439170.1:p.Arg429Ser
ENST00000642339.1:c.*831G>C	ENSP00000495425.1:n.*831G>C
ENST00000642431.1:c.1711G>C
ENST00000642463.1:c.*1032G>C	ENSP00000495007.1:n.*1032G>C
ENST00000642503.1:c.*908G>C	ENSP00000494334.1:n.*908G>C
ENST00000642610.2:c.1134G>C MANE Select	ENSP00000494796.1:p.Arg378Ser
ENST00000642764.1:n.1965G>C
ENST00000643125.1:c.*149G>C	ENSP00000494102.1:n.*149G>C
ENST00000643142.1:c.*625G>C	ENSP00000494755.1:n.*625G>C
ENST00000643238.1:c.*154G>C	ENSP00000495916.1:n.*154G>C
ENST00000643410.1:c.*424G>C	ENSP00000495030.1:n.*424G>C
ENST00000643487.1:n.1821G>C
ENST00000643524.1:c.*719G>C	ENSP00000494026.1:n.*719G>C
ENST00000643615.1:c.*1116+1312G>C	ENSP00000496103.1:n.*1116+1312G>C
ENST00000643993.1:n.1270G>C
ENST00000643994.1:c.*1134G>C	ENSP00000496322.1:n.*1134G>C
ENST00000644037.1:c.*1344G>C	ENSP00000496408.1:n.*1344G>C
ENST00000644055.1:c.*1759G>C	ENSP00000496307.1:n.*1759G>C
ENST00000644126.1:n.2806G>C
ENST00000644217.1:c.1134G>C	ENSP00000494646.1:p.Arg378Ser
ENST00000644265.1:c.503G>C
ENST00000644578.1:c.948G>C	ENSP00000495953.1:p.Arg316Ser
ENST00000644604.1:c.1134G>C	ENSP00000495961.1:p.Arg378Ser
ENST00000644680.1:c.*1655G>C	ENSP00000496173.1:n.*1655G>C
ENST00000644838.1:c.*517G>C	ENSP00000495910.1:n.*517G>C
ENST00000644910.1:c.1741G>C
ENST00000645205.1:c.1134G>C	ENSP00000495823.1:p.Arg378Ser
ENST00000645351.1:c.1134G>C	ENSP00000494319.1:p.Arg378Ser
ENST00000645551.1:c.*851G>C	ENSP00000495928.1:n.*851G>C
ENST00000645578.1:c.*908G>C	ENSP00000496495.1:n.*908G>C
ENST00000645582.1:c.*964G>C	ENSP00000494980.1:n.*964G>C
ENST00000645655.1:c.1134G>C	ENSP00000495202.1:p.Arg378Ser
ENST00000645662.1:c.*593G>C	ENSP00000495964.1:n.*593G>C
ENST00000645836.1:c.*908G>C	ENSP00000493915.1:n.*908G>C
ENST00000645899.1:c.1134G>C	ENSP00000496773.1:p.Arg378Ser
ENST00000645964.1:c.*1000G>C	ENSP00000494208.1:n.*1000G>C
ENST00000646104.1:c.*1602G>C	ENSP00000495475.1:n.*1602G>C
ENST00000646186.1:c.*806G>C	ENSP00000493806.1:n.*806G>C
ENST00000646286.1:c.*1027G>C	ENSP00000494291.1:n.*1027G>C
ENST00000646463.1:c.*899G>C	ENSP00000494541.1:n.*899G>C
ENST00000646528.1:c.*1850G>C	ENSP00000496553.1:n.*1850G>C
ENST00000646536.1:c.*424G>C	ENSP00000494801.1:n.*424G>C
ENST00000646624.1:c.1134G>C	ENSP00000494575.1:p.Arg378Ser
ENST00000646821.1:c.*424G>C	ENSP00000495257.1:n.*424G>C
ENST00000646842.1:n.578G>C
ENST00000646848.1:c.*349G>C	ENSP00000495831.1:n.*349G>C
ENST00000647186.1:c.1134G>C	ENSP00000494775.1:p.Arg378Ser
ENST00000647233.1:n.2114G>C
ENST00000647322.1:c.725G>C
ENST00000647418.1:c.*908G>C	ENSP00000493552.1:n.*908G>C
ENST00000647428.1:c.795G>C	ENSP00000495630.1:p.Arg265Ser
ENST00000651186.1:c.795G>C	ENSP00000498645.1:p.Arg265Ser
ENST00000366601.7:c.1134G>C	ENSP00000355560.3:p.Arg378Ser
ENST00000406207.4:c.1134G>C	ENSP00000384571.1:p.Arg378Ser
ENST00000472011.5:n.1186G>C
ENST00000543662.3:c.1287G>C	ENSP00000439170.1:p.Arg429Ser
NM_001079515.2:c.1134G>C	NP_001072983.1:p.Arg378Ser
NM_001287801.1:c.1287G>C	NP_001274730.1:p.Arg429Ser
NM_001287802.1:c.795G>C	NP_001274731.1:p.Arg265Ser
NM_003193.4:c.1134G>C	NP_003184.1:p.Arg378Ser
NM_003193.5:c.1134G>C MANE Select	NP_003184.1:p.Arg378Ser
NM_001079515.3:c.1134G>C	NP_001072983.1:p.Arg378Ser
NM_001287801.2:c.1287G>C	NP_001274730.1:p.Arg429Ser
NM_001287802.2:c.795G>C	NP_001274731.1:p.Arg265Ser