Canonical Allele Identifier: CA1522545855
Gene: TERT HGNC NCBI

Linked Data

dbSNP Id: rs1748630478

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1266680_1266683del , CM000667.2:g.1266680_1266683del GRCh38
NC_000005.9:g.1266795_1266798del , CM000667.1:g.1266795_1266798del GRCh37
NC_000005.8:g.1319795_1319798del NCBI36
NG_009265.1:g.33369_33372del , LRG_343:g.33369_33372del

Transcript Alleles

HGVS Amino-acid Change
ENST00000310581.10:c.2583-144_2583-141del MANE Select ENSP00000309572.5:n.2583-144_2583-141del
ENST00000656021.1:c.*2129-144_*2129-141del ENSP00000499759.1:n.*2129-144_*2129-141del
ENST00000310581.9:c.2583-144_2583-141del ENSP00000309572.5:n.2583-144_2583-141del
ENST00000334602.10:c.2583-144_2583-141del ENSP00000334346.6:n.2583-144_2583-141del
ENST00000460137.6:c.2365-144_2365-141del ENSP00000425003.1:n.2365-144_2365-141del
ENST00000484238.6:n.1214-144_1214-141del
ENST00000508104.2:c.2401-144_2401-141del ENSP00000426042.2:n.2401-144_2401-141del
NM_001193376.1:c.2583-144_2583-141del NP_001180305.1:n.2583-144_2583-141del
NM_198253.2:c.2583-144_2583-141del , LRG_343t1:c.2583-144_2583-141del NP_937983.2:n.2583-144_2583-141del
XM_011514104.1:c.1053-144_1053-141del XP_011512406.1:n.1053-144_1053-141del
XM_011514105.1:c.939-144_939-141del XP_011512407.1:n.939-144_939-141del
XM_011514106.1:c.939-144_939-141del XP_011512408.1:n.939-144_939-141del
NR_149162.1:n.2459-144_2459-141del
NR_149163.1:n.2423-144_2423-141del
NM_001193376.2:c.2583-144_2583-141del NP_001180305.1:n.2583-144_2583-141del
NM_198253.3:c.2583-144_2583-141del MANE Select NP_937983.2:n.2583-144_2583-141del
NR_149162.2:n.2480-144_2480-141del
NR_149163.2:n.2444-144_2444-141del
NM_001193376.3:c.2583-144_2583-141del NP_001180305.1:n.2583-144_2583-141del
NR_149162.3:n.2480-144_2480-141del
NR_149163.3:n.2444-144_2444-141del