Canonical Allele Identifier: CA1072505586

Gene: TERT

Linked Data

• dbSNP Id: rs2126631968
• gnomAD v3: 5-1275742-T-TCCCACACATGAAAACCAATCCCACAGATCCCCACCTAC
• gnomAD v4: 5-1275742-T-TCCCACACATGAAAACCAATCCCACAGATCCCCACCTAC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1275771_1275772insCCCACCTACCCCACACATGAAAACCAATCCCACAGATC , CM000667.2:g.1275771_1275772insCCCACCTACCCCACACATGAAAACCAATCCCACAGATC	GRCh38
NC_000005.9:g.1275886_1275887insCCCACCTACCCCACACATGAAAACCAATCCCACAGATC , CM000667.1:g.1275886_1275887insCCCACCTACCCCACACATGAAAACCAATCCCACAGATC	GRCh37
NC_000005.8:g.1328886_1328887insCCCACCTACCCCACACATGAAAACCAATCCCACAGATC	NCBI36
NG_009265.1:g.24305_24306insGTAGGTGGGGATCTGTGGGATTGGTTTTCATGTGTGGG , LRG_343:g.24305_24306insGTAGGTGGGGATCTGTGGGATTGGTTTTCATGTGTGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310581.10:c.2286+2898_2286+2899insGTAGGTGGGGATCTGTGGGATTGGTTTTCATGTGTGGG MANE Select	ENSP00000309572.5:n.2286+2898_2286+2899insGTAGGTGGGGATCTGTGGG...
ENST00000656021.1:c.*1832+2898_*1832+2899insGTAGGTGGGGATCTGTGGGATTGGTTTTCATGTGTGGG	ENSP00000499759.1:n.*1832+2898_*1832+2899insGTAGGTGGGGATCTGTG...
ENST00000310581.9:c.2286+2898_2286+2899insGTAGGTGGGGATCTGTGGGATTGGTTTTCATGTGTGGG	ENSP00000309572.5:n.2286+2898_2286+2899insGTAGGTGGGGATCTGTGGG...
ENST00000334602.10:c.2286+2898_2286+2899insGTAGGTGGGGATCTGTGGGATTGGTTTTCATGTGTGGG	ENSP00000334346.6:n.2286+2898_2286+2899insGTAGGTGGGGATCTGTGGG...
ENST00000460137.6:c.2250+2898_2250+2899insGTAGGTGGGGATCTGTGGGATTGGTTTTCATGTGTGGG	ENSP00000425003.1:n.2250+2898_2250+2899insGTAGGTGGGGATCTGTGGG...
ENST00000484238.6:n.1099+2898_1099+2899insGTAGGTGGGGATCTGTGGGATTGGTTTTCATGTGTGGG
ENST00000508104.2:c.2286+2898_2286+2899insGTAGGTGGGGATCTGTGGGATTGGTTTTCATGTGTGGG	ENSP00000426042.2:n.2286+2898_2286+2899insGTAGGTGGGGATCTGTGGG...
NM_001193376.1:c.2286+2898_2286+2899insGTAGGTGGGGATCTGTGGGATTGGTTTTCATGTGTGGG	NP_001180305.1:n.2286+2898_2286+2899insGTAGGTGGGGATCTGTGGGATT...
NM_198253.2:c.2286+2898_2286+2899insGTAGGTGGGGATCTGTGGGATTGGTTTTCATGTGTGGG , LRG_343t1:c.2286+2898_2286+2899insGTAGGTGGGGATCTGTGGGATTGGTTTTCATGTGTGGG	NP_937983.2:n.2286+2898_2286+2899insGTAGGTGGGGATCTGTGGGATTGGT...
XM_011514104.1:c.756+2898_756+2899insGTAGGTGGGGATCTGTGGGATTGGTTTTCATGTGTGGG	XP_011512406.1:n.756+2898_756+2899insGTAGGTGGGGATCTGTGGGATTGG...
XM_011514105.1:c.642+2898_642+2899insGTAGGTGGGGATCTGTGGGATTGGTTTTCATGTGTGGG	XP_011512407.1:n.642+2898_642+2899insGTAGGTGGGGATCTGTGGGATTGG...
XM_011514106.1:c.642+2898_642+2899insGTAGGTGGGGATCTGTGGGATTGGTTTTCATGTGTGGG	XP_011512408.1:n.642+2898_642+2899insGTAGGTGGGGATCTGTGGGATTGG...
NR_149162.1:n.2344+2898_2344+2899insGTAGGTGGGGATCTGTGGGATTGGTTTTCATGTGTGGG
NR_149163.1:n.2308+2898_2308+2899insGTAGGTGGGGATCTGTGGGATTGGTTTTCATGTGTGGG
NM_001193376.2:c.2286+2898_2286+2899insGTAGGTGGGGATCTGTGGGATTGGTTTTCATGTGTGGG	NP_001180305.1:n.2286+2898_2286+2899insGTAGGTGGGGATCTGTGGGATT...
NM_198253.3:c.2286+2898_2286+2899insGTAGGTGGGGATCTGTGGGATTGGTTTTCATGTGTGGG MANE Select	NP_937983.2:n.2286+2898_2286+2899insGTAGGTGGGGATCTGTGGGATTGGT...
NR_149162.2:n.2365+2898_2365+2899insGTAGGTGGGGATCTGTGGGATTGGTTTTCATGTGTGGG
NR_149163.2:n.2329+2898_2329+2899insGTAGGTGGGGATCTGTGGGATTGGTTTTCATGTGTGGG
NM_001193376.3:c.2286+2898_2286+2899insGTAGGTGGGGATCTGTGGGATTGGTTTTCATGTGTGGG	NP_001180305.1:n.2286+2898_2286+2899insGTAGGTGGGGATCTGTGGGATT...
NR_149162.3:n.2365+2898_2365+2899insGTAGGTGGGGATCTGTGGGATTGGTTTTCATGTGTGGG
NR_149163.3:n.2329+2898_2329+2899insGTAGGTGGGGATCTGTGGGATTGGTTTTCATGTGTGGG