Canonical Allele Identifier: CA1522539322

Gene: TERT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1260029_1260065delinsAGGGCTGCAGCTTCAGAGCCTCAGCCCACCAAGGCCT , CM000667.2:g.1260029_1260065delinsAGGGCTGCAGCTTCAGAGCCTCAGCCCACCAAGGCCT	GRCh38
NC_000005.9:g.1260144_1260180delinsAGGGCTGCAGCTTCAGAGCCTCAGCCCACCAAGGCCT , CM000667.1:g.1260144_1260180delinsAGGGCTGCAGCTTCAGAGCCTCAGCCCACCAAGGCCT	GRCh37
NC_000005.8:g.1313144_1313180delinsAGGGCTGCAGCTTCAGAGCCTCAGCCCACCAAGGCCT	NCBI36
NG_009265.1:g.39983_40019delinsAGGCCTTGGTGGGCTGAGGCTCTGAAGCTGCAGCCCT , LRG_343:g.39983_40019delinsAGGCCTTGGTGGGCTGAGGCTCTGAAGCTGCAGCCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310581.10:c.2970+409_2970+445delinsAGGCCTTGGTGGGCTGAGGCTCTGAAGCTGCAGCCCT MANE Select	ENSP00000309572.5:n.2970+409_2970+445delinsAGGCCTTGGTGGGCTGAG...
ENST00000656021.1:c.*2516+409_*2516+445delinsAGGCCTTGGTGGGCTGAGGCTCTGAAGCTGCAGCCCT	ENSP00000499759.1:n.*2516+409_*2516+445delinsAGGCCTTGGTGGGCTG...
ENST00000667927.1:n.258+409_258+445delinsAGGCCTTGGTGGGCTGAGGCTCTGAAGCTGCAGCCCT
ENST00000310581.9:c.2970+409_2970+445delinsAGGCCTTGGTGGGCTGAGGCTCTGAAGCTGCAGCCCT	ENSP00000309572.5:n.2970+409_2970+445delinsAGGCCTTGGTGGGCTGAG...
ENST00000334602.10:c.2781+409_2781+445delinsAGGCCTTGGTGGGCTGAGGCTCTGAAGCTGCAGCCCT	ENSP00000334346.6:n.2781+409_2781+445delinsAGGCCTTGGTGGGCTGAG...
ENST00000460137.6:c.2563+409_2563+445delinsAGGCCTTGGTGGGCTGAGGCTCTGAAGCTGCAGCCCT	ENSP00000425003.1:n.2563+409_2563+445delinsAGGCCTTGGTGGGCTGAG...
ENST00000484238.6:n.1412+409_1412+445delinsAGGCCTTGGTGGGCTGAGGCTCTGAAGCTGCAGCCCT
NM_001193376.1:c.2781+409_2781+445delinsAGGCCTTGGTGGGCTGAGGCTCTGAAGCTGCAGCCCT	NP_001180305.1:n.2781+409_2781+445delinsAGGCCTTGGTGGGCTGAGGCT...
NM_198253.2:c.2970+409_2970+445delinsAGGCCTTGGTGGGCTGAGGCTCTGAAGCTGCAGCCCT , LRG_343t1:c.2970+409_2970+445delinsAGGCCTTGGTGGGCTGAGGCTCTGAAGCTGCAGCCCT	NP_937983.2:n.2970+409_2970+445delinsAGGCCTTGGTGGGCTGAGGCTCTG...
XM_011514104.1:c.1440+409_1440+445delinsAGGCCTTGGTGGGCTGAGGCTCTGAAGCTGCAGCCCT	XP_011512406.1:n.1440+409_1440+445delinsAGGCCTTGGTGGGCTGAGGCT...
XM_011514105.1:c.1326+409_1326+445delinsAGGCCTTGGTGGGCTGAGGCTCTGAAGCTGCAGCCCT	XP_011512407.1:n.1326+409_1326+445delinsAGGCCTTGGTGGGCTGAGGCT...
XM_011514106.1:c.1326+409_1326+445delinsAGGCCTTGGTGGGCTGAGGCTCTGAAGCTGCAGCCCT	XP_011512408.1:n.1326+409_1326+445delinsAGGCCTTGGTGGGCTGAGGCT...
NR_149162.1:n.2657+409_2657+445delinsAGGCCTTGGTGGGCTGAGGCTCTGAAGCTGCAGCCCT
NR_149163.1:n.2621+409_2621+445delinsAGGCCTTGGTGGGCTGAGGCTCTGAAGCTGCAGCCCT
NM_001193376.2:c.2781+409_2781+445delinsAGGCCTTGGTGGGCTGAGGCTCTGAAGCTGCAGCCCT	NP_001180305.1:n.2781+409_2781+445delinsAGGCCTTGGTGGGCTGAGGCT...
NM_198253.3:c.2970+409_2970+445delinsAGGCCTTGGTGGGCTGAGGCTCTGAAGCTGCAGCCCT MANE Select	NP_937983.2:n.2970+409_2970+445delinsAGGCCTTGGTGGGCTGAGGCTCTG...
NR_149162.2:n.2678+409_2678+445delinsAGGCCTTGGTGGGCTGAGGCTCTGAAGCTGCAGCCCT
NR_149163.2:n.2642+409_2642+445delinsAGGCCTTGGTGGGCTGAGGCTCTGAAGCTGCAGCCCT
NM_001193376.3:c.2781+409_2781+445delinsAGGCCTTGGTGGGCTGAGGCTCTGAAGCTGCAGCCCT	NP_001180305.1:n.2781+409_2781+445delinsAGGCCTTGGTGGGCTGAGGCT...
NR_149162.3:n.2678+409_2678+445delinsAGGCCTTGGTGGGCTGAGGCTCTGAAGCTGCAGCCCT
NR_149163.3:n.2642+409_2642+445delinsAGGCCTTGGTGGGCTGAGGCTCTGAAGCTGCAGCCCT