Canonical Allele Identifier: CA1072505709
Gene: TERT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1275790_1275804del , CM000667.2:g.1275790_1275804del GRCh38
NC_000005.9:g.1275905_1275919del , CM000667.1:g.1275905_1275919del GRCh37
NC_000005.8:g.1328905_1328919del NCBI36
NG_009265.1:g.24244_24258del , LRG_343:g.24244_24258del

Transcript Alleles

HGVS Amino-acid Change
ENST00000310581.10:c.2286+2837_2286+2851del MANE Select ENSP00000309572.5:n.2286+2837_2286+2851del
ENST00000656021.1:c.*1832+2837_*1832+2851del ENSP00000499759.1:n.*1832+2837_*1832+2851del
ENST00000310581.9:c.2286+2837_2286+2851del ENSP00000309572.5:n.2286+2837_2286+2851del
ENST00000334602.10:c.2286+2837_2286+2851del ENSP00000334346.6:n.2286+2837_2286+2851del
ENST00000460137.6:c.2250+2837_2250+2851del ENSP00000425003.1:n.2250+2837_2250+2851del
ENST00000484238.6:n.1099+2837_1099+2851del
ENST00000508104.2:c.2286+2837_2286+2851del ENSP00000426042.2:n.2286+2837_2286+2851del
NM_001193376.1:c.2286+2837_2286+2851del NP_001180305.1:n.2286+2837_2286+2851del
NM_198253.2:c.2286+2837_2286+2851del , LRG_343t1:c.2286+2837_2286+2851del NP_937983.2:n.2286+2837_2286+2851del
XM_011514104.1:c.756+2837_756+2851del XP_011512406.1:n.756+2837_756+2851del
XM_011514105.1:c.642+2837_642+2851del XP_011512407.1:n.642+2837_642+2851del
XM_011514106.1:c.642+2837_642+2851del XP_011512408.1:n.642+2837_642+2851del
NR_149162.1:n.2344+2837_2344+2851del
NR_149163.1:n.2308+2837_2308+2851del
NM_001193376.2:c.2286+2837_2286+2851del NP_001180305.1:n.2286+2837_2286+2851del
NM_198253.3:c.2286+2837_2286+2851del MANE Select NP_937983.2:n.2286+2837_2286+2851del
NR_149162.2:n.2365+2837_2365+2851del
NR_149163.2:n.2329+2837_2329+2851del
NM_001193376.3:c.2286+2837_2286+2851del NP_001180305.1:n.2286+2837_2286+2851del
NR_149162.3:n.2365+2837_2365+2851del
NR_149163.3:n.2329+2837_2329+2851del