Canonical Allele Identifier: CA1522582218

Gene: TERT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1293277_1293278delinsTG , CM000667.2:g.1293277_1293278delinsTG	GRCh38
NC_000005.9:g.1293392_1293393delinsTG , CM000667.1:g.1293392_1293393delinsTG	GRCh37
NC_000005.8:g.1346392_1346393delinsTG	NCBI36
NG_009265.1:g.6770_6771delinsCA , LRG_343:g.6770_6771delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310581.10:c.1573+35_1573+36delinsCA MANE Select	ENSP00000309572.5:n.1573+35_1573+36delinsCA
ENST00000656021.1:c.1608_1609delinsCA	ENSP00000499759.1:p.Pro536=
ENST00000310581.9:c.1573+35_1573+36delinsCA	ENSP00000309572.5:n.1573+35_1573+36delinsCA
ENST00000334602.10:c.1573+35_1573+36delinsCA	ENSP00000334346.6:n.1573+35_1573+36delinsCA
ENST00000460137.6:c.1573+35_1573+36delinsCA	ENSP00000425003.1:n.1573+35_1573+36delinsCA
ENST00000508104.2:c.1573+35_1573+36delinsCA	ENSP00000426042.2:n.1573+35_1573+36delinsCA
NM_001193376.1:c.1573+35_1573+36delinsCA	NP_001180305.1:n.1573+35_1573+36delinsCA
NM_198253.2:c.1573+35_1573+36delinsCA , LRG_343t1:c.1573+35_1573+36delinsCA	NP_937983.2:n.1573+35_1573+36delinsCA
NR_149162.1:n.1631+35_1631+36delinsCA
NR_149163.1:n.1631+35_1631+36delinsCA
NM_001193376.2:c.1573+35_1573+36delinsCA	NP_001180305.1:n.1573+35_1573+36delinsCA
NM_198253.3:c.1573+35_1573+36delinsCA MANE Select	NP_937983.2:n.1573+35_1573+36delinsCA
NR_149162.2:n.1652+35_1652+36delinsCA
NR_149163.2:n.1652+35_1652+36delinsCA
NM_001193376.3:c.1573+35_1573+36delinsCA	NP_001180305.1:n.1573+35_1573+36delinsCA
NR_149162.3:n.1652+35_1652+36delinsCA
NR_149163.3:n.1652+35_1652+36delinsCA