Canonical Allele Identifier: CA803452897
Gene: TERT HGNC NCBI

Linked Data

dbSNP Id: rs1470677169

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1271955_1271956del , CM000667.2:g.1271955_1271956del GRCh38
NC_000005.9:g.1272070_1272071del , CM000667.1:g.1272070_1272071del GRCh37
NC_000005.8:g.1325070_1325071del NCBI36
NG_009265.1:g.28097_28098del , LRG_343:g.28097_28098del

Transcript Alleles

HGVS Amino-acid Change
ENST00000310581.10:c.2382+234_2382+235del MANE Select ENSP00000309572.5:n.2382+234_2382+235del
ENST00000656021.1:c.*1928+234_*1928+235del ENSP00000499759.1:n.*1928+234_*1928+235del
ENST00000310581.9:c.2382+234_2382+235del ENSP00000309572.5:n.2382+234_2382+235del
ENST00000334602.10:c.2382+234_2382+235del ENSP00000334346.6:n.2382+234_2382+235del
ENST00000460137.6:c.2251-3318_2251-3317del ENSP00000425003.1:n.2251-3318_2251-3317del
ENST00000484238.6:n.1100-3318_1100-3317del
ENST00000508104.2:c.2287-3318_2287-3317del ENSP00000426042.2:n.2287-3318_2287-3317del
NM_001193376.1:c.2382+234_2382+235del NP_001180305.1:n.2382+234_2382+235del
NM_198253.2:c.2382+234_2382+235del , LRG_343t1:c.2382+234_2382+235del NP_937983.2:n.2382+234_2382+235del
XM_011514104.1:c.852+234_852+235del XP_011512406.1:n.852+234_852+235del
XM_011514105.1:c.738+234_738+235del XP_011512407.1:n.738+234_738+235del
XM_011514106.1:c.738+234_738+235del XP_011512408.1:n.738+234_738+235del
NR_149162.1:n.2345-3318_2345-3317del
NR_149163.1:n.2309-3318_2309-3317del
NM_001193376.2:c.2382+234_2382+235del NP_001180305.1:n.2382+234_2382+235del
NM_198253.3:c.2382+234_2382+235del MANE Select NP_937983.2:n.2382+234_2382+235del
NR_149162.2:n.2366-3318_2366-3317del
NR_149163.2:n.2330-3318_2330-3317del
NM_001193376.3:c.2382+234_2382+235del NP_001180305.1:n.2382+234_2382+235del
NR_149162.3:n.2366-3318_2366-3317del
NR_149163.3:n.2330-3318_2330-3317del