Canonical Allele Identifier: CA1072505633
Gene: TERT HGNC NCBI

Linked Data

dbSNP Id: rs1749522163

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1275772_1275809del , CM000667.2:g.1275772_1275809del GRCh38
NC_000005.9:g.1275887_1275924del , CM000667.1:g.1275887_1275924del GRCh37
NC_000005.8:g.1328887_1328924del NCBI36
NG_009265.1:g.24248_24285del , LRG_343:g.24248_24285del

Transcript Alleles

HGVS Amino-acid Change
ENST00000310581.10:c.2286+2841_2286+2878del MANE Select ENSP00000309572.5:n.2286+2841_2286+2878del
ENST00000656021.1:c.*1832+2841_*1832+2878del ENSP00000499759.1:n.*1832+2841_*1832+2878del
ENST00000310581.9:c.2286+2841_2286+2878del ENSP00000309572.5:n.2286+2841_2286+2878del
ENST00000334602.10:c.2286+2841_2286+2878del ENSP00000334346.6:n.2286+2841_2286+2878del
ENST00000460137.6:c.2250+2841_2250+2878del ENSP00000425003.1:n.2250+2841_2250+2878del
ENST00000484238.6:n.1099+2841_1099+2878del
ENST00000508104.2:c.2286+2841_2286+2878del ENSP00000426042.2:n.2286+2841_2286+2878del
NM_001193376.1:c.2286+2841_2286+2878del NP_001180305.1:n.2286+2841_2286+2878del
NM_198253.2:c.2286+2841_2286+2878del , LRG_343t1:c.2286+2841_2286+2878del NP_937983.2:n.2286+2841_2286+2878del
XM_011514104.1:c.756+2841_756+2878del XP_011512406.1:n.756+2841_756+2878del
XM_011514105.1:c.642+2841_642+2878del XP_011512407.1:n.642+2841_642+2878del
XM_011514106.1:c.642+2841_642+2878del XP_011512408.1:n.642+2841_642+2878del
NR_149162.1:n.2344+2841_2344+2878del
NR_149163.1:n.2308+2841_2308+2878del
NM_001193376.2:c.2286+2841_2286+2878del NP_001180305.1:n.2286+2841_2286+2878del
NM_198253.3:c.2286+2841_2286+2878del MANE Select NP_937983.2:n.2286+2841_2286+2878del
NR_149162.2:n.2365+2841_2365+2878del
NR_149163.2:n.2329+2841_2329+2878del
NM_001193376.3:c.2286+2841_2286+2878del NP_001180305.1:n.2286+2841_2286+2878del
NR_149162.3:n.2365+2841_2365+2878del
NR_149163.3:n.2329+2841_2329+2878del