Canonical Allele Identifier: CA1522545514

Gene: TERT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1266404_1266405delinsGC , CM000667.2:g.1266404_1266405delinsGC	GRCh38
NC_000005.9:g.1266519_1266520delinsGC , CM000667.1:g.1266519_1266520delinsGC	GRCh37
NC_000005.8:g.1319519_1319520delinsGC	NCBI36
NG_009265.1:g.33643_33644delinsGC , LRG_343:g.33643_33644delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310581.10:c.2654+59_2654+60delinsGC MANE Select	ENSP00000309572.5:n.2654+59_2654+60delinsGC
ENST00000656021.1:c.*2200+59_*2200+60delinsGC	ENSP00000499759.1:n.*2200+59_*2200+60delinsGC
ENST00000310581.9:c.2654+59_2654+60delinsGC	ENSP00000309572.5:n.2654+59_2654+60delinsGC
ENST00000334602.10:c.2654+59_2654+60delinsGC	ENSP00000334346.6:n.2654+59_2654+60delinsGC
ENST00000460137.6:c.2436+59_2436+60delinsGC	ENSP00000425003.1:n.2436+59_2436+60delinsGC
ENST00000484238.6:n.1285+59_1285+60delinsGC
ENST00000503656.1:n.61+59_61+60delinsGC
NM_001193376.1:c.2654+59_2654+60delinsGC	NP_001180305.1:n.2654+59_2654+60delinsGC
NM_198253.2:c.2654+59_2654+60delinsGC , LRG_343t1:c.2654+59_2654+60delinsGC	NP_937983.2:n.2654+59_2654+60delinsGC
XM_011514104.1:c.1124+59_1124+60delinsGC	XP_011512406.1:n.1124+59_1124+60delinsGC
XM_011514105.1:c.1010+59_1010+60delinsGC	XP_011512407.1:n.1010+59_1010+60delinsGC
XM_011514106.1:c.1010+59_1010+60delinsGC	XP_011512408.1:n.1010+59_1010+60delinsGC
NR_149162.1:n.2530+59_2530+60delinsGC
NR_149163.1:n.2494+59_2494+60delinsGC
NM_001193376.2:c.2654+59_2654+60delinsGC	NP_001180305.1:n.2654+59_2654+60delinsGC
NM_198253.3:c.2654+59_2654+60delinsGC MANE Select	NP_937983.2:n.2654+59_2654+60delinsGC
NR_149162.2:n.2551+59_2551+60delinsGC
NR_149163.2:n.2515+59_2515+60delinsGC
NM_001193376.3:c.2654+59_2654+60delinsGC	NP_001180305.1:n.2654+59_2654+60delinsGC
NR_149162.3:n.2551+59_2551+60delinsGC
NR_149163.3:n.2515+59_2515+60delinsGC