Canonical Allele Identifier: CA1522555390

Gene: TERT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1293600_1293601delinsTC , CM000667.2:g.1293600_1293601delinsTC	GRCh38
NC_000005.9:g.1293715_1293716delinsTC , CM000667.1:g.1293715_1293716delinsTC	GRCh37
NC_000005.8:g.1346715_1346716delinsTC	NCBI36
NG_009265.1:g.6447_6448delinsGA , LRG_343:g.6447_6448delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310581.10:c.1285_1286delinsGA MANE Select	ENSP00000309572.5:p.Glu429=
ENST00000656021.1:c.1285_1286delinsGA	ENSP00000499759.1:p.Glu429=
ENST00000310581.9:c.1285_1286delinsGA	ENSP00000309572.5:p.Glu429=
ENST00000334602.10:c.1285_1286delinsGA	ENSP00000334346.6:p.Glu429=
ENST00000460137.6:c.1285_1286delinsGA	ENSP00000425003.1:p.Glu429=
ENST00000508104.2:c.1285_1286delinsGA	ENSP00000426042.2:p.Glu429=
NM_001193376.1:c.1285_1286delinsGA	NP_001180305.1:p.Glu429=
NM_198253.2:c.1285_1286delinsGA , LRG_343t1:c.1285_1286delinsGA	NP_937983.2:p.Glu429=
NR_149162.1:n.1343_1344delinsGA
NR_149163.1:n.1343_1344delinsGA
NM_001193376.2:c.1285_1286delinsGA	NP_001180305.1:p.Glu429=
NM_198253.3:c.1285_1286delinsGA MANE Select	NP_937983.2:p.Glu429=
NR_149162.2:n.1364_1365delinsGA
NR_149163.2:n.1364_1365delinsGA
NM_001193376.3:c.1285_1286delinsGA	NP_001180305.1:p.Glu429=
NR_149162.3:n.1364_1365delinsGA
NR_149163.3:n.1364_1365delinsGA