Canonical Allele Identifier: CA1522545506

Gene: TERT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1266398_1266399delinsCG , CM000667.2:g.1266398_1266399delinsCG	GRCh38
NC_000005.9:g.1266513_1266514delinsCG , CM000667.1:g.1266513_1266514delinsCG	GRCh37
NC_000005.8:g.1319513_1319514delinsCG	NCBI36
NG_009265.1:g.33649_33650delinsCG , LRG_343:g.33649_33650delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310581.10:c.2654+65_2654+66delinsCG MANE Select	ENSP00000309572.5:n.2654+65_2654+66delinsCG
ENST00000656021.1:c.*2200+65_*2200+66delinsCG	ENSP00000499759.1:n.*2200+65_*2200+66delinsCG
ENST00000310581.9:c.2654+65_2654+66delinsCG	ENSP00000309572.5:n.2654+65_2654+66delinsCG
ENST00000334602.10:c.2654+65_2654+66delinsCG	ENSP00000334346.6:n.2654+65_2654+66delinsCG
ENST00000460137.6:c.2436+65_2436+66delinsCG	ENSP00000425003.1:n.2436+65_2436+66delinsCG
ENST00000484238.6:n.1285+65_1285+66delinsCG
ENST00000503656.1:n.61+65_61+66delinsCG
NM_001193376.1:c.2654+65_2654+66delinsCG	NP_001180305.1:n.2654+65_2654+66delinsCG
NM_198253.2:c.2654+65_2654+66delinsCG , LRG_343t1:c.2654+65_2654+66delinsCG	NP_937983.2:n.2654+65_2654+66delinsCG
XM_011514104.1:c.1124+65_1124+66delinsCG	XP_011512406.1:n.1124+65_1124+66delinsCG
XM_011514105.1:c.1010+65_1010+66delinsCG	XP_011512407.1:n.1010+65_1010+66delinsCG
XM_011514106.1:c.1010+65_1010+66delinsCG	XP_011512408.1:n.1010+65_1010+66delinsCG
NR_149162.1:n.2530+65_2530+66delinsCG
NR_149163.1:n.2494+65_2494+66delinsCG
NM_001193376.2:c.2654+65_2654+66delinsCG	NP_001180305.1:n.2654+65_2654+66delinsCG
NM_198253.3:c.2654+65_2654+66delinsCG MANE Select	NP_937983.2:n.2654+65_2654+66delinsCG
NR_149162.2:n.2551+65_2551+66delinsCG
NR_149163.2:n.2515+65_2515+66delinsCG
NM_001193376.3:c.2654+65_2654+66delinsCG	NP_001180305.1:n.2654+65_2654+66delinsCG
NR_149162.3:n.2551+65_2551+66delinsCG
NR_149163.3:n.2515+65_2515+66delinsCG