Canonical Allele Identifier: CA1522539473
Gene: TERT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1260205_1260207delinsCCA , CM000667.2:g.1260205_1260207delinsCCA GRCh38
NC_000005.9:g.1260320_1260322delinsCCA , CM000667.1:g.1260320_1260322delinsCCA GRCh37
NC_000005.8:g.1313320_1313322delinsCCA NCBI36
NG_009265.1:g.39841_39843delinsTGG , LRG_343:g.39841_39843delinsTGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000310581.10:c.2970+267_2970+269delinsTGG MANE Select ENSP00000309572.5:n.2970+267_2970+269delinsTGG
ENST00000656021.1:c.*2516+267_*2516+269delinsTGG ENSP00000499759.1:n.*2516+267_*2516+269delinsTGG
ENST00000667927.1:n.258+267_258+269delinsTGG
ENST00000310581.9:c.2970+267_2970+269delinsTGG ENSP00000309572.5:n.2970+267_2970+269delinsTGG
ENST00000334602.10:c.2781+267_2781+269delinsTGG ENSP00000334346.6:n.2781+267_2781+269delinsTGG
ENST00000460137.6:c.2563+267_2563+269delinsTGG ENSP00000425003.1:n.2563+267_2563+269delinsTGG
ENST00000484238.6:n.1412+267_1412+269delinsTGG
NM_001193376.1:c.2781+267_2781+269delinsTGG NP_001180305.1:n.2781+267_2781+269delinsTGG
NM_198253.2:c.2970+267_2970+269delinsTGG , LRG_343t1:c.2970+267_2970+269delinsTGG NP_937983.2:n.2970+267_2970+269delinsTGG
XM_011514104.1:c.1440+267_1440+269delinsTGG XP_011512406.1:n.1440+267_1440+269delinsTGG
XM_011514105.1:c.1326+267_1326+269delinsTGG XP_011512407.1:n.1326+267_1326+269delinsTGG
XM_011514106.1:c.1326+267_1326+269delinsTGG XP_011512408.1:n.1326+267_1326+269delinsTGG
NR_149162.1:n.2657+267_2657+269delinsTGG
NR_149163.1:n.2621+267_2621+269delinsTGG
NM_001193376.2:c.2781+267_2781+269delinsTGG NP_001180305.1:n.2781+267_2781+269delinsTGG
NM_198253.3:c.2970+267_2970+269delinsTGG MANE Select NP_937983.2:n.2970+267_2970+269delinsTGG
NR_149162.2:n.2678+267_2678+269delinsTGG
NR_149163.2:n.2642+267_2642+269delinsTGG
NM_001193376.3:c.2781+267_2781+269delinsTGG NP_001180305.1:n.2781+267_2781+269delinsTGG
NR_149162.3:n.2678+267_2678+269delinsTGG
NR_149163.3:n.2642+267_2642+269delinsTGG