Canonical Allele Identifier: CA1522539482

Gene: TERT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1260213_1260215delinsCTG , CM000667.2:g.1260213_1260215delinsCTG	GRCh38
NC_000005.9:g.1260328_1260330delinsCTG , CM000667.1:g.1260328_1260330delinsCTG	GRCh37
NC_000005.8:g.1313328_1313330delinsCTG	NCBI36
NG_009265.1:g.39833_39835delinsCAG , LRG_343:g.39833_39835delinsCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310581.10:c.2970+259_2970+261delinsCAG MANE Select	ENSP00000309572.5:n.2970+259_2970+261delinsCAG
ENST00000656021.1:c.*2516+259_*2516+261delinsCAG	ENSP00000499759.1:n.*2516+259_*2516+261delinsCAG
ENST00000667927.1:n.258+259_258+261delinsCAG
ENST00000310581.9:c.2970+259_2970+261delinsCAG	ENSP00000309572.5:n.2970+259_2970+261delinsCAG
ENST00000334602.10:c.2781+259_2781+261delinsCAG	ENSP00000334346.6:n.2781+259_2781+261delinsCAG
ENST00000460137.6:c.2563+259_2563+261delinsCAG	ENSP00000425003.1:n.2563+259_2563+261delinsCAG
ENST00000484238.6:n.1412+259_1412+261delinsCAG
NM_001193376.1:c.2781+259_2781+261delinsCAG	NP_001180305.1:n.2781+259_2781+261delinsCAG
NM_198253.2:c.2970+259_2970+261delinsCAG , LRG_343t1:c.2970+259_2970+261delinsCAG	NP_937983.2:n.2970+259_2970+261delinsCAG
XM_011514104.1:c.1440+259_1440+261delinsCAG	XP_011512406.1:n.1440+259_1440+261delinsCAG
XM_011514105.1:c.1326+259_1326+261delinsCAG	XP_011512407.1:n.1326+259_1326+261delinsCAG
XM_011514106.1:c.1326+259_1326+261delinsCAG	XP_011512408.1:n.1326+259_1326+261delinsCAG
NR_149162.1:n.2657+259_2657+261delinsCAG
NR_149163.1:n.2621+259_2621+261delinsCAG
NM_001193376.2:c.2781+259_2781+261delinsCAG	NP_001180305.1:n.2781+259_2781+261delinsCAG
NM_198253.3:c.2970+259_2970+261delinsCAG MANE Select	NP_937983.2:n.2970+259_2970+261delinsCAG
NR_149162.2:n.2678+259_2678+261delinsCAG
NR_149163.2:n.2642+259_2642+261delinsCAG
NM_001193376.3:c.2781+259_2781+261delinsCAG	NP_001180305.1:n.2781+259_2781+261delinsCAG
NR_149162.3:n.2678+259_2678+261delinsCAG
NR_149163.3:n.2642+259_2642+261delinsCAG