Canonical Allele Identifier: CA2673080621
Gene: TERT HGNC NCBI

Linked Data

gnomAD v4: 5-1293673-AG-A

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1293677del , CM000667.2:g.1293677del GRCh38
NC_000005.9:g.1293792del , CM000667.1:g.1293792del GRCh37
NC_000005.8:g.1346792del NCBI36
NG_009265.1:g.6374del , LRG_343:g.6374del

Transcript Alleles

HGVS Amino-acid change
ENST00000310581.10:c.1212del MANE Select ENSP00000309572.5:p.Tyr405ThrfsTer?
ENST00000656021.1:c.1212del ENSP00000499759.1:p.Tyr405ThrfsTer?
ENST00000310581.9:c.1212del ENSP00000309572.5:p.Tyr405ThrfsTer?
ENST00000334602.10:c.1212del ENSP00000334346.6:p.Tyr405ThrfsTer?
ENST00000460137.6:c.1212del ENSP00000425003.1:p.Tyr405ThrfsTer?
ENST00000508104.2:c.1212del ENSP00000426042.2:p.Tyr405ThrfsTer?
NM_001193376.1:c.1212del NP_001180305.1:p.Tyr405ThrfsTer?
NM_198253.2:c.1212del , LRG_343t1:c.1212del NP_937983.2:p.Tyr405ThrfsTer?
NR_149162.1:n.1270del
NR_149163.1:n.1270del
NM_001193376.2:c.1212del NP_001180305.1:p.Tyr405ThrfsTer?
NM_198253.3:c.1212del MANE Select NP_937983.2:p.Tyr405ThrfsTer?
NR_149162.2:n.1291del
NR_149163.2:n.1291del
NM_001193376.3:c.1212del NP_001180305.1:p.Tyr405ThrfsTer?
NR_149162.3:n.1291del
NR_149163.3:n.1291del