Canonical Allele Identifier: CA1522539455

Gene: TERT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1260188_1260193delinsGCACCT , CM000667.2:g.1260188_1260193delinsGCACCT	GRCh38
NC_000005.9:g.1260303_1260308delinsGCACCT , CM000667.1:g.1260303_1260308delinsGCACCT	GRCh37
NC_000005.8:g.1313303_1313308delinsGCACCT	NCBI36
NG_009265.1:g.39855_39860delinsAGGTGC , LRG_343:g.39855_39860delinsAGGTGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310581.10:c.2970+281_2970+286delinsAGGTGC MANE Select	ENSP00000309572.5:n.2970+281_2970+286delinsAGGTGC
ENST00000656021.1:c.*2516+281_*2516+286delinsAGGTGC	ENSP00000499759.1:n.*2516+281_*2516+286delinsAGGTGC
ENST00000667927.1:n.258+281_258+286delinsAGGTGC
ENST00000310581.9:c.2970+281_2970+286delinsAGGTGC	ENSP00000309572.5:n.2970+281_2970+286delinsAGGTGC
ENST00000334602.10:c.2781+281_2781+286delinsAGGTGC	ENSP00000334346.6:n.2781+281_2781+286delinsAGGTGC
ENST00000460137.6:c.2563+281_2563+286delinsAGGTGC	ENSP00000425003.1:n.2563+281_2563+286delinsAGGTGC
ENST00000484238.6:n.1412+281_1412+286delinsAGGTGC
NM_001193376.1:c.2781+281_2781+286delinsAGGTGC	NP_001180305.1:n.2781+281_2781+286delinsAGGTGC
NM_198253.2:c.2970+281_2970+286delinsAGGTGC , LRG_343t1:c.2970+281_2970+286delinsAGGTGC	NP_937983.2:n.2970+281_2970+286delinsAGGTGC
XM_011514104.1:c.1440+281_1440+286delinsAGGTGC	XP_011512406.1:n.1440+281_1440+286delinsAGGTGC
XM_011514105.1:c.1326+281_1326+286delinsAGGTGC	XP_011512407.1:n.1326+281_1326+286delinsAGGTGC
XM_011514106.1:c.1326+281_1326+286delinsAGGTGC	XP_011512408.1:n.1326+281_1326+286delinsAGGTGC
NR_149162.1:n.2657+281_2657+286delinsAGGTGC
NR_149163.1:n.2621+281_2621+286delinsAGGTGC
NM_001193376.2:c.2781+281_2781+286delinsAGGTGC	NP_001180305.1:n.2781+281_2781+286delinsAGGTGC
NM_198253.3:c.2970+281_2970+286delinsAGGTGC MANE Select	NP_937983.2:n.2970+281_2970+286delinsAGGTGC
NR_149162.2:n.2678+281_2678+286delinsAGGTGC
NR_149163.2:n.2642+281_2642+286delinsAGGTGC
NM_001193376.3:c.2781+281_2781+286delinsAGGTGC	NP_001180305.1:n.2781+281_2781+286delinsAGGTGC
NR_149162.3:n.2678+281_2678+286delinsAGGTGC
NR_149163.3:n.2642+281_2642+286delinsAGGTGC