Canonical Allele Identifier: CA1522555100

Gene: TERT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1293505_1293508delinsCCTG , CM000667.2:g.1293505_1293508delinsCCTG	GRCh38
NC_000005.9:g.1293620_1293623delinsCCTG , CM000667.1:g.1293620_1293623delinsCCTG	GRCh37
NC_000005.8:g.1346620_1346623delinsCCTG	NCBI36
NG_009265.1:g.6540_6543delinsCAGG , LRG_343:g.6540_6543delinsCAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310581.10:c.1378_1381delinsCAGG MANE Select	ENSP00000309572.5:p.Gln460=
ENST00000656021.1:c.1378_1381delinsCAGG	ENSP00000499759.1:p.Gln460=
ENST00000310581.9:c.1378_1381delinsCAGG	ENSP00000309572.5:p.Gln460=
ENST00000334602.10:c.1378_1381delinsCAGG	ENSP00000334346.6:p.Gln460=
ENST00000460137.6:c.1378_1381delinsCAGG	ENSP00000425003.1:p.Gln460=
ENST00000508104.2:c.1378_1381delinsCAGG	ENSP00000426042.2:p.Gln460=
NM_001193376.1:c.1378_1381delinsCAGG	NP_001180305.1:p.Gln460=
NM_198253.2:c.1378_1381delinsCAGG , LRG_343t1:c.1378_1381delinsCAGG	NP_937983.2:p.Gln460=
NR_149162.1:n.1436_1439delinsCAGG
NR_149163.1:n.1436_1439delinsCAGG
NM_001193376.2:c.1378_1381delinsCAGG	NP_001180305.1:p.Gln460=
NM_198253.3:c.1378_1381delinsCAGG MANE Select	NP_937983.2:p.Gln460=
NR_149162.2:n.1457_1460delinsCAGG
NR_149163.2:n.1457_1460delinsCAGG
NM_001193376.3:c.1378_1381delinsCAGG	NP_001180305.1:p.Gln460=
NR_149162.3:n.1457_1460delinsCAGG
NR_149163.3:n.1457_1460delinsCAGG