Canonical Allele Identifier: CA1522560541

Gene: TERT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1275714_1275752delinsAAAAACCAATCCCACAGATCCCCACCTATCCCACACATG , CM000667.2:g.1275714_1275752delinsAAAAACCAATCCCACAGATCCCCACCTATCCCACACATG	GRCh38
NC_000005.9:g.1275829_1275867delinsAAAAACCAATCCCACAGATCCCCACCTATCCCACACATG , CM000667.1:g.1275829_1275867delinsAAAAACCAATCCCACAGATCCCCACCTATCCCACACATG	GRCh37
NC_000005.8:g.1328829_1328867delinsAAAAACCAATCCCACAGATCCCCACCTATCCCACACATG	NCBI36
NG_009265.1:g.24296_24334delinsCATGTGTGGGATAGGTGGGGATCTGTGGGATTGGTTTTT , LRG_343:g.24296_24334delinsCATGTGTGGGATAGGTGGGGATCTGTGGGATTGGTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310581.10:c.2286+2889_2286+2927delinsCATGTGTGGGATAGGTGGGGATCTGTGGGATTGGTTTTT MANE Select	ENSP00000309572.5:n.2286+2889_2286+2927delinsCATGTGTGGGATAGGT...
ENST00000656021.1:c.*1832+2889_*1832+2927delinsCATGTGTGGGATAGGTGGGGATCTGTGGGATTGGTTTTT	ENSP00000499759.1:n.*1832+2889_*1832+2927delinsCATGTGTGGGATAG...
ENST00000310581.9:c.2286+2889_2286+2927delinsCATGTGTGGGATAGGTGGGGATCTGTGGGATTGGTTTTT	ENSP00000309572.5:n.2286+2889_2286+2927delinsCATGTGTGGGATAGGT...
ENST00000334602.10:c.2286+2889_2286+2927delinsCATGTGTGGGATAGGTGGGGATCTGTGGGATTGGTTTTT	ENSP00000334346.6:n.2286+2889_2286+2927delinsCATGTGTGGGATAGGT...
ENST00000460137.6:c.2250+2889_2250+2927delinsCATGTGTGGGATAGGTGGGGATCTGTGGGATTGGTTTTT	ENSP00000425003.1:n.2250+2889_2250+2927delinsCATGTGTGGGATAGGT...
ENST00000484238.6:n.1099+2889_1099+2927delinsCATGTGTGGGATAGGTGGGGATCTGTGGGATTGGTTTTT
ENST00000508104.2:c.2286+2889_2286+2927delinsCATGTGTGGGATAGGTGGGGATCTGTGGGATTGGTTTTT	ENSP00000426042.2:n.2286+2889_2286+2927delinsCATGTGTGGGATAGGT...
NM_001193376.1:c.2286+2889_2286+2927delinsCATGTGTGGGATAGGTGGGGATCTGTGGGATTGGTTTTT	NP_001180305.1:n.2286+2889_2286+2927delinsCATGTGTGGGATAGGTGGG...
NM_198253.2:c.2286+2889_2286+2927delinsCATGTGTGGGATAGGTGGGGATCTGTGGGATTGGTTTTT , LRG_343t1:c.2286+2889_2286+2927delinsCATGTGTGGGATAGGTGGGGATCTGTGGGATTGGTTTTT	NP_937983.2:n.2286+2889_2286+2927delinsCATGTGTGGGATAGGTGGGGAT...
XM_011514104.1:c.756+2889_756+2927delinsCATGTGTGGGATAGGTGGGGATCTGTGGGATTGGTTTTT	XP_011512406.1:n.756+2889_756+2927delinsCATGTGTGGGATAGGTGGGGA...
XM_011514105.1:c.642+2889_642+2927delinsCATGTGTGGGATAGGTGGGGATCTGTGGGATTGGTTTTT	XP_011512407.1:n.642+2889_642+2927delinsCATGTGTGGGATAGGTGGGGA...
XM_011514106.1:c.642+2889_642+2927delinsCATGTGTGGGATAGGTGGGGATCTGTGGGATTGGTTTTT	XP_011512408.1:n.642+2889_642+2927delinsCATGTGTGGGATAGGTGGGGA...
NR_149162.1:n.2344+2889_2344+2927delinsCATGTGTGGGATAGGTGGGGATCTGTGGGATTGGTTTTT
NR_149163.1:n.2308+2889_2308+2927delinsCATGTGTGGGATAGGTGGGGATCTGTGGGATTGGTTTTT
NM_001193376.2:c.2286+2889_2286+2927delinsCATGTGTGGGATAGGTGGGGATCTGTGGGATTGGTTTTT	NP_001180305.1:n.2286+2889_2286+2927delinsCATGTGTGGGATAGGTGGG...
NM_198253.3:c.2286+2889_2286+2927delinsCATGTGTGGGATAGGTGGGGATCTGTGGGATTGGTTTTT MANE Select	NP_937983.2:n.2286+2889_2286+2927delinsCATGTGTGGGATAGGTGGGGAT...
NR_149162.2:n.2365+2889_2365+2927delinsCATGTGTGGGATAGGTGGGGATCTGTGGGATTGGTTTTT
NR_149163.2:n.2329+2889_2329+2927delinsCATGTGTGGGATAGGTGGGGATCTGTGGGATTGGTTTTT
NM_001193376.3:c.2286+2889_2286+2927delinsCATGTGTGGGATAGGTGGGGATCTGTGGGATTGGTTTTT	NP_001180305.1:n.2286+2889_2286+2927delinsCATGTGTGGGATAGGTGGG...
NR_149162.3:n.2365+2889_2365+2927delinsCATGTGTGGGATAGGTGGGGATCTGTGGGATTGGTTTTT
NR_149163.3:n.2329+2889_2329+2927delinsCATGTGTGGGATAGGTGGGGATCTGTGGGATTGGTTTTT