Canonical Allele Identifier: CA1522539467

Gene: TERT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1260203_1260204delinsGC , CM000667.2:g.1260203_1260204delinsGC	GRCh38
NC_000005.9:g.1260318_1260319delinsGC , CM000667.1:g.1260318_1260319delinsGC	GRCh37
NC_000005.8:g.1313318_1313319delinsGC	NCBI36
NG_009265.1:g.39844_39845delinsGC , LRG_343:g.39844_39845delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310581.10:c.2970+270_2970+271delinsGC MANE Select	ENSP00000309572.5:n.2970+270_2970+271delinsGC
ENST00000656021.1:c.*2516+270_*2516+271delinsGC	ENSP00000499759.1:n.*2516+270_*2516+271delinsGC
ENST00000667927.1:n.258+270_258+271delinsGC
ENST00000310581.9:c.2970+270_2970+271delinsGC	ENSP00000309572.5:n.2970+270_2970+271delinsGC
ENST00000334602.10:c.2781+270_2781+271delinsGC	ENSP00000334346.6:n.2781+270_2781+271delinsGC
ENST00000460137.6:c.2563+270_2563+271delinsGC	ENSP00000425003.1:n.2563+270_2563+271delinsGC
ENST00000484238.6:n.1412+270_1412+271delinsGC
NM_001193376.1:c.2781+270_2781+271delinsGC	NP_001180305.1:n.2781+270_2781+271delinsGC
NM_198253.2:c.2970+270_2970+271delinsGC , LRG_343t1:c.2970+270_2970+271delinsGC	NP_937983.2:n.2970+270_2970+271delinsGC
XM_011514104.1:c.1440+270_1440+271delinsGC	XP_011512406.1:n.1440+270_1440+271delinsGC
XM_011514105.1:c.1326+270_1326+271delinsGC	XP_011512407.1:n.1326+270_1326+271delinsGC
XM_011514106.1:c.1326+270_1326+271delinsGC	XP_011512408.1:n.1326+270_1326+271delinsGC
NR_149162.1:n.2657+270_2657+271delinsGC
NR_149163.1:n.2621+270_2621+271delinsGC
NM_001193376.2:c.2781+270_2781+271delinsGC	NP_001180305.1:n.2781+270_2781+271delinsGC
NM_198253.3:c.2970+270_2970+271delinsGC MANE Select	NP_937983.2:n.2970+270_2970+271delinsGC
NR_149162.2:n.2678+270_2678+271delinsGC
NR_149163.2:n.2642+270_2642+271delinsGC
NM_001193376.3:c.2781+270_2781+271delinsGC	NP_001180305.1:n.2781+270_2781+271delinsGC
NR_149162.3:n.2678+270_2678+271delinsGC
NR_149163.3:n.2642+270_2642+271delinsGC