Canonical Allele Identifier: CA2765040137

Gene: TERT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1260401_1260402insGCAC , CM000667.2:g.1260401_1260402insGCAC	GRCh38
NC_000005.9:g.1260516_1260517insGCAC , CM000667.1:g.1260516_1260517insGCAC	GRCh37
NC_000005.8:g.1313516_1313517insGCAC	NCBI36
NG_009265.1:g.39647_39648insTGCG , LRG_343:g.39647_39648insTGCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310581.10:c.2970+73_2970+74insTGCG MANE Select	ENSP00000309572.5:n.2970+73_2970+74insTGCG
ENST00000656021.1:c.*2516+73_*2516+74insTGCG	ENSP00000499759.1:n.*2516+73_*2516+74insTGCG
ENST00000667927.1:n.258+73_258+74insTGCG
ENST00000310581.9:c.2970+73_2970+74insTGCG	ENSP00000309572.5:n.2970+73_2970+74insTGCG
ENST00000334602.10:c.2781+73_2781+74insTGCG	ENSP00000334346.6:n.2781+73_2781+74insTGCG
ENST00000460137.6:c.2563+73_2563+74insTGCG	ENSP00000425003.1:n.2563+73_2563+74insTGCG
ENST00000484238.6:n.1412+73_1412+74insTGCG
NM_001193376.1:c.2781+73_2781+74insTGCG	NP_001180305.1:n.2781+73_2781+74insTGCG
NM_198253.2:c.2970+73_2970+74insTGCG , LRG_343t1:c.2970+73_2970+74insTGCG	NP_937983.2:n.2970+73_2970+74insTGCG
XM_011514104.1:c.1440+73_1440+74insTGCG	XP_011512406.1:n.1440+73_1440+74insTGCG
XM_011514105.1:c.1326+73_1326+74insTGCG	XP_011512407.1:n.1326+73_1326+74insTGCG
XM_011514106.1:c.1326+73_1326+74insTGCG	XP_011512408.1:n.1326+73_1326+74insTGCG
NR_149162.1:n.2657+73_2657+74insTGCG
NR_149163.1:n.2621+73_2621+74insTGCG
NM_001193376.2:c.2781+73_2781+74insTGCG	NP_001180305.1:n.2781+73_2781+74insTGCG
NM_198253.3:c.2970+73_2970+74insTGCG MANE Select	NP_937983.2:n.2970+73_2970+74insTGCG
NR_149162.2:n.2678+73_2678+74insTGCG
NR_149163.2:n.2642+73_2642+74insTGCG
NM_001193376.3:c.2781+73_2781+74insTGCG	NP_001180305.1:n.2781+73_2781+74insTGCG
NR_149162.3:n.2678+73_2678+74insTGCG
NR_149163.3:n.2642+73_2642+74insTGCG