Canonical Allele Identifier: CA1522560590
Gene: TERT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1275742_1275818delinsTCCCACACATGAAAACCAATCCCACAGATCTCCACCTACCCCACACATGAAAACCAACTCCACAGATCCCCACCTAC , CM000667.2:g.1275742_1275818delinsTCCCACACATGAAAACCAATCCCACAGATCTCCACCTACCCCACACATGAAAACCAACTCCACAGATCCCCACCTAC GRCh38
NC_000005.9:g.1275857_1275933delinsTCCCACACATGAAAACCAATCCCACAGATCTCCACCTACCCCACACATGAAAACCAACTCCACAGATCCCCACCTAC , CM000667.1:g.1275857_1275933delinsTCCCACACATGAAAACCAATCCCACAGATCTCCACCTACCCCACACATGAAAACCAACTCCACAGATCCCCACCTAC GRCh37
NC_000005.8:g.1328857_1328933delinsTCCCACACATGAAAACCAATCCCACAGATCTCCACCTACCCCACACATGAAAACCAACTCCACAGATCCCCACCTAC NCBI36
NG_009265.1:g.24230_24306delinsGTAGGTGGGGATCTGTGGAGTTGGTTTTCATGTGTGGGGTAGGTGGAGATCTGTGGGATTGGTTTTCATGTGTGGGA , LRG_343:g.24230_24306delinsGTAGGTGGGGATCTGTGGAGTTGGTTTTCATGTGTGGGGTAGGTGGAGATCTGTGGGATTGGTTTTCATGTGTGGGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000310581.10:c.2286+2823_2286+2899delinsGTAGGTGGGGATCTGTGGAGTTGGTTTTCATGTGTGGGGTAGGTGGAGATCTGTGGGATTGGTTTTCATGTGTGGGA MANE Select ENSP00000309572.5:n.2286+2823_2286+2899delinsGTAGGTGGGGATCTGT...
ENST00000656021.1:c.*1832+2823_*1832+2899delinsGTAGGTGGGGATCTGTGGAGTTGGTTTTCATGTGTGGGGTAGGTGGAGATCTGTGGGATTGGTTTTCATGTGTGGGA ENSP00000499759.1:n.*1832+2823_*1832+2899delinsGTAGGTGGGGATCT...
ENST00000310581.9:c.2286+2823_2286+2899delinsGTAGGTGGGGATCTGTGGAGTTGGTTTTCATGTGTGGGGTAGGTGGAGATCTGTGGGATTGGTTTTCATGTGTGGGA ENSP00000309572.5:n.2286+2823_2286+2899delinsGTAGGTGGGGATCTGT...
ENST00000334602.10:c.2286+2823_2286+2899delinsGTAGGTGGGGATCTGTGGAGTTGGTTTTCATGTGTGGGGTAGGTGGAGATCTGTGGGATTGGTTTTCATGTGTGGGA ENSP00000334346.6:n.2286+2823_2286+2899delinsGTAGGTGGGGATCTGT...
ENST00000460137.6:c.2250+2823_2250+2899delinsGTAGGTGGGGATCTGTGGAGTTGGTTTTCATGTGTGGGGTAGGTGGAGATCTGTGGGATTGGTTTTCATGTGTGGGA ENSP00000425003.1:n.2250+2823_2250+2899delinsGTAGGTGGGGATCTGT...
ENST00000484238.6:n.1099+2823_1099+2899delinsGTAGGTGGGGATCTGTGGAGTTGGTTTTCATGTGTGGGGTAGGTGGAGATCTGTGGGATTGGTTTTCATGTGTGGGA
ENST00000508104.2:c.2286+2823_2286+2899delinsGTAGGTGGGGATCTGTGGAGTTGGTTTTCATGTGTGGGGTAGGTGGAGATCTGTGGGATTGGTTTTCATGTGTGGGA ENSP00000426042.2:n.2286+2823_2286+2899delinsGTAGGTGGGGATCTGT...
NM_001193376.1:c.2286+2823_2286+2899delinsGTAGGTGGGGATCTGTGGAGTTGGTTTTCATGTGTGGGGTAGGTGGAGATCTGTGGGATTGGTTTTCATGTGTGGGA NP_001180305.1:n.2286+2823_2286+2899delinsGTAGGTGGGGATCTGTGGA...
NM_198253.2:c.2286+2823_2286+2899delinsGTAGGTGGGGATCTGTGGAGTTGGTTTTCATGTGTGGGGTAGGTGGAGATCTGTGGGATTGGTTTTCATGTGTGGGA , LRG_343t1:c.2286+2823_2286+2899delinsGTAGGTGGGGATCTGTGGAGTTGGTTTTCATGTGTGGGGTAGGTGGAGATCTGTGGGATTGGTTTTCATGTGTGGGA NP_937983.2:n.2286+2823_2286+2899delinsGTAGGTGGGGATCTGTGGAGTT...
XM_011514104.1:c.756+2823_756+2899delinsGTAGGTGGGGATCTGTGGAGTTGGTTTTCATGTGTGGGGTAGGTGGAGATCTGTGGGATTGGTTTTCATGTGTGGGA XP_011512406.1:n.756+2823_756+2899delinsGTAGGTGGGGATCTGTGGAGT...
XM_011514105.1:c.642+2823_642+2899delinsGTAGGTGGGGATCTGTGGAGTTGGTTTTCATGTGTGGGGTAGGTGGAGATCTGTGGGATTGGTTTTCATGTGTGGGA XP_011512407.1:n.642+2823_642+2899delinsGTAGGTGGGGATCTGTGGAGT...
XM_011514106.1:c.642+2823_642+2899delinsGTAGGTGGGGATCTGTGGAGTTGGTTTTCATGTGTGGGGTAGGTGGAGATCTGTGGGATTGGTTTTCATGTGTGGGA XP_011512408.1:n.642+2823_642+2899delinsGTAGGTGGGGATCTGTGGAGT...
NR_149162.1:n.2344+2823_2344+2899delinsGTAGGTGGGGATCTGTGGAGTTGGTTTTCATGTGTGGGGTAGGTGGAGATCTGTGGGATTGGTTTTCATGTGTGGGA
NR_149163.1:n.2308+2823_2308+2899delinsGTAGGTGGGGATCTGTGGAGTTGGTTTTCATGTGTGGGGTAGGTGGAGATCTGTGGGATTGGTTTTCATGTGTGGGA
NM_001193376.2:c.2286+2823_2286+2899delinsGTAGGTGGGGATCTGTGGAGTTGGTTTTCATGTGTGGGGTAGGTGGAGATCTGTGGGATTGGTTTTCATGTGTGGGA NP_001180305.1:n.2286+2823_2286+2899delinsGTAGGTGGGGATCTGTGGA...
NM_198253.3:c.2286+2823_2286+2899delinsGTAGGTGGGGATCTGTGGAGTTGGTTTTCATGTGTGGGGTAGGTGGAGATCTGTGGGATTGGTTTTCATGTGTGGGA MANE Select NP_937983.2:n.2286+2823_2286+2899delinsGTAGGTGGGGATCTGTGGAGTT...
NR_149162.2:n.2365+2823_2365+2899delinsGTAGGTGGGGATCTGTGGAGTTGGTTTTCATGTGTGGGGTAGGTGGAGATCTGTGGGATTGGTTTTCATGTGTGGGA
NR_149163.2:n.2329+2823_2329+2899delinsGTAGGTGGGGATCTGTGGAGTTGGTTTTCATGTGTGGGGTAGGTGGAGATCTGTGGGATTGGTTTTCATGTGTGGGA
NM_001193376.3:c.2286+2823_2286+2899delinsGTAGGTGGGGATCTGTGGAGTTGGTTTTCATGTGTGGGGTAGGTGGAGATCTGTGGGATTGGTTTTCATGTGTGGGA NP_001180305.1:n.2286+2823_2286+2899delinsGTAGGTGGGGATCTGTGGA...
NR_149162.3:n.2365+2823_2365+2899delinsGTAGGTGGGGATCTGTGGAGTTGGTTTTCATGTGTGGGGTAGGTGGAGATCTGTGGGATTGGTTTTCATGTGTGGGA
NR_149163.3:n.2329+2823_2329+2899delinsGTAGGTGGGGATCTGTGGAGTTGGTTTTCATGTGTGGGGTAGGTGGAGATCTGTGGGATTGGTTTTCATGTGTGGGA