Canonical Allele Identifier: CA2673079556
Gene: TERT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1279547_1279551del , CM000667.2:g.1279547_1279551del GRCh38
NC_000005.9:g.1279662_1279666del , CM000667.1:g.1279662_1279666del GRCh37
NC_000005.8:g.1332662_1332666del NCBI36
NG_009265.1:g.20498_20502del , LRG_343:g.20498_20502del

Transcript Alleles

HGVS Amino-acid Change
ENST00000310581.10:c.1951-80_1951-76del MANE Select ENSP00000309572.5:n.1951-80_1951-76del
ENST00000656021.1:c.*1497-80_*1497-76del ENSP00000499759.1:n.*1497-80_*1497-76del
ENST00000310581.9:c.1951-80_1951-76del ENSP00000309572.5:n.1951-80_1951-76del
ENST00000334602.10:c.1951-80_1951-76del ENSP00000334346.6:n.1951-80_1951-76del
ENST00000460137.6:c.1951-80_1951-76del ENSP00000425003.1:n.1951-80_1951-76del
ENST00000484238.6:n.764-80_764-76del
ENST00000508104.2:c.1951-80_1951-76del ENSP00000426042.2:n.1951-80_1951-76del
NM_001193376.1:c.1951-80_1951-76del NP_001180305.1:n.1951-80_1951-76del
NM_198253.2:c.1951-80_1951-76del , LRG_343t1:c.1951-80_1951-76del NP_937983.2:n.1951-80_1951-76del
XM_011514104.1:c.421-80_421-76del XP_011512406.1:n.421-80_421-76del
XM_011514105.1:c.307-80_307-76del XP_011512407.1:n.307-80_307-76del
XM_011514106.1:c.307-80_307-76del XP_011512408.1:n.307-80_307-76del
NR_149162.1:n.2009-80_2009-76del
NR_149163.1:n.2009-80_2009-76del
NM_001193376.2:c.1951-80_1951-76del NP_001180305.1:n.1951-80_1951-76del
NM_198253.3:c.1951-80_1951-76del MANE Select NP_937983.2:n.1951-80_1951-76del
NR_149162.2:n.2030-80_2030-76del
NR_149163.2:n.2030-80_2030-76del
NM_001193376.3:c.1951-80_1951-76del NP_001180305.1:n.1951-80_1951-76del
NR_149162.3:n.2030-80_2030-76del
NR_149163.3:n.2030-80_2030-76del