Canonical Allele Identifier: CA423771603

Gene: TBCE

Linked Data

• MyVariant Identifiers: chr1:g.235602105A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.235438790A>C , CM000663.2:g.235438790A>C	GRCh38
NC_000001.10:g.235602105A>C , CM000663.1:g.235602105A>C	GRCh37
NC_000001.9:g.233668728A>C	NCBI36
NG_009230.1:g.76378A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366601.8:c.949A>C	ENSP00000355560.4:p.Arg317=
ENST00000406207.5:c.1138A>C	ENSP00000384571.1:p.Arg380=
ENST00000472011.6:n.1862A>C
ENST00000543662.4:c.1291A>C	ENSP00000439170.1:p.Arg431=
ENST00000642339.1:c.*835A>C	ENSP00000495425.1:n.*835A>C
ENST00000642431.1:c.1715A>C
ENST00000642463.1:c.*1036A>C	ENSP00000495007.1:n.*1036A>C
ENST00000642503.1:c.*912A>C	ENSP00000494334.1:n.*912A>C
ENST00000642610.2:c.1138A>C MANE Select	ENSP00000494796.1:p.Arg380=
ENST00000642764.1:n.1969A>C
ENST00000643125.1:c.*153A>C	ENSP00000494102.1:n.*153A>C
ENST00000643142.1:c.*629A>C	ENSP00000494755.1:n.*629A>C
ENST00000643238.1:c.*158A>C	ENSP00000495916.1:n.*158A>C
ENST00000643410.1:c.*428A>C	ENSP00000495030.1:n.*428A>C
ENST00000643487.1:n.1825A>C
ENST00000643524.1:c.*723A>C	ENSP00000494026.1:n.*723A>C
ENST00000643615.1:c.*1116+1316A>C	ENSP00000496103.1:n.*1116+1316A>C
ENST00000643993.1:n.1274A>C
ENST00000643994.1:c.*1138A>C	ENSP00000496322.1:n.*1138A>C
ENST00000644037.1:c.*1348A>C	ENSP00000496408.1:n.*1348A>C
ENST00000644055.1:c.*1763A>C	ENSP00000496307.1:n.*1763A>C
ENST00000644126.1:n.2810A>C
ENST00000644217.1:c.1138A>C	ENSP00000494646.1:p.Arg380=
ENST00000644265.1:c.507A>C
ENST00000644578.1:c.952A>C	ENSP00000495953.1:p.Arg318=
ENST00000644604.1:c.1138A>C	ENSP00000495961.1:p.Arg380=
ENST00000644680.1:c.*1659A>C	ENSP00000496173.1:n.*1659A>C
ENST00000644838.1:c.*521A>C	ENSP00000495910.1:n.*521A>C
ENST00000644910.1:c.1745A>C
ENST00000645205.1:c.1138A>C	ENSP00000495823.1:p.Arg380=
ENST00000645351.1:c.1138A>C	ENSP00000494319.1:p.Arg380=
ENST00000645551.1:c.*855A>C	ENSP00000495928.1:n.*855A>C
ENST00000645578.1:c.*912A>C	ENSP00000496495.1:n.*912A>C
ENST00000645582.1:c.*968A>C	ENSP00000494980.1:n.*968A>C
ENST00000645655.1:c.1138A>C	ENSP00000495202.1:p.Arg380=
ENST00000645662.1:c.*597A>C	ENSP00000495964.1:n.*597A>C
ENST00000645836.1:c.*912A>C	ENSP00000493915.1:n.*912A>C
ENST00000645899.1:c.1138A>C	ENSP00000496773.1:p.Arg380=
ENST00000645964.1:c.*1004A>C	ENSP00000494208.1:n.*1004A>C
ENST00000646104.1:c.*1606A>C	ENSP00000495475.1:n.*1606A>C
ENST00000646186.1:c.*810A>C	ENSP00000493806.1:n.*810A>C
ENST00000646286.1:c.*1031A>C	ENSP00000494291.1:n.*1031A>C
ENST00000646463.1:c.*903A>C	ENSP00000494541.1:n.*903A>C
ENST00000646528.1:c.*1854A>C	ENSP00000496553.1:n.*1854A>C
ENST00000646536.1:c.*428A>C	ENSP00000494801.1:n.*428A>C
ENST00000646624.1:c.1138A>C	ENSP00000494575.1:p.Arg380=
ENST00000646821.1:c.*428A>C	ENSP00000495257.1:n.*428A>C
ENST00000646842.1:n.582A>C
ENST00000646848.1:c.*353A>C	ENSP00000495831.1:n.*353A>C
ENST00000647186.1:c.1138A>C	ENSP00000494775.1:p.Arg380=
ENST00000647233.1:n.2118A>C
ENST00000647322.1:c.729A>C
ENST00000647418.1:c.*912A>C	ENSP00000493552.1:n.*912A>C
ENST00000647428.1:c.799A>C	ENSP00000495630.1:p.Arg267=
ENST00000651186.1:c.799A>C	ENSP00000498645.1:p.Arg267=
ENST00000366601.7:c.1138A>C	ENSP00000355560.3:p.Arg380=
ENST00000406207.4:c.1138A>C	ENSP00000384571.1:p.Arg380=
ENST00000472011.5:n.1190A>C
ENST00000543662.3:c.1291A>C	ENSP00000439170.1:p.Arg431=
NM_001079515.2:c.1138A>C	NP_001072983.1:p.Arg380=
NM_001287801.1:c.1291A>C	NP_001274730.1:p.Arg431=
NM_001287802.1:c.799A>C	NP_001274731.1:p.Arg267=
NM_003193.4:c.1138A>C	NP_003184.1:p.Arg380=
NM_003193.5:c.1138A>C MANE Select	NP_003184.1:p.Arg380=
NM_001079515.3:c.1138A>C	NP_001072983.1:p.Arg380=
NM_001287801.2:c.1291A>C	NP_001274730.1:p.Arg431=
NM_001287802.2:c.799A>C	NP_001274731.1:p.Arg267=