Canonical Allele Identifier: CA2983076868
Gene: TERT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1293554del , CM000667.2:g.1293554del GRCh38
NC_000005.9:g.1293669del , CM000667.1:g.1293669del GRCh37
NC_000005.8:g.1346669del NCBI36
NG_009265.1:g.6498del , LRG_343:g.6498del

Transcript Alleles

HGVS Amino-acid Change
ENST00000310581.10:c.1336del MANE Select ENSP00000309572.5:p.Arg446ValfsTer?
ENST00000656021.1:c.1336del ENSP00000499759.1:p.Arg446ValfsTer?
ENST00000310581.9:c.1336del ENSP00000309572.5:p.Arg446ValfsTer?
ENST00000334602.10:c.1336del ENSP00000334346.6:p.Arg446ValfsTer?
ENST00000460137.6:c.1336del ENSP00000425003.1:p.Arg446ValfsTer?
ENST00000508104.2:c.1336del ENSP00000426042.2:p.Arg446ValfsTer?
NM_001193376.1:c.1336del NP_001180305.1:p.Arg446ValfsTer?
NM_198253.2:c.1336del , LRG_343t1:c.1336del NP_937983.2:p.Arg446ValfsTer?
NR_149162.1:n.1394del
NR_149163.1:n.1394del
NM_001193376.2:c.1336del NP_001180305.1:p.Arg446ValfsTer?
NM_198253.3:c.1336del MANE Select NP_937983.2:p.Arg446ValfsTer?
NR_149162.2:n.1415del
NR_149163.2:n.1415del
NM_001193376.3:c.1336del NP_001180305.1:p.Arg446ValfsTer?
NR_149162.3:n.1415del
NR_149163.3:n.1415del