Canonical Allele Identifier: CA2708195421
Gene: TERT HGNC NCBI

Linked Data

dbSNP Id: rs2126643022

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1279704_1279706del , CM000667.2:g.1279704_1279706del GRCh38
NC_000005.9:g.1279819_1279821del , CM000667.1:g.1279819_1279821del GRCh37
NC_000005.8:g.1332819_1332821del NCBI36
NG_009265.1:g.20345_20347del , LRG_343:g.20345_20347del

Transcript Alleles

HGVS Amino-acid change
ENST00000310581.10:c.1951-233_1951-231del MANE Select ENSP00000309572.5:n.1951-233_1951-231del
ENST00000656021.1:c.*1497-233_*1497-231del ENSP00000499759.1:n.*1497-233_*1497-231de...
ENST00000310581.9:c.1951-233_1951-231del ENSP00000309572.5:n.1951-233_1951-231del
ENST00000334602.10:c.1951-233_1951-231del ENSP00000334346.6:n.1951-233_1951-231del
ENST00000460137.6:c.1951-233_1951-231del ENSP00000425003.1:n.1951-233_1951-231del
ENST00000484238.6:n.764-233_764-231del
ENST00000508104.2:c.1951-233_1951-231del ENSP00000426042.2:n.1951-233_1951-231del
NM_001193376.1:c.1951-233_1951-231del NP_001180305.1:n.1951-233_1951-231del
NM_198253.2:c.1951-233_1951-231del , LRG_343t1:c.1951-233_1951-231del NP_937983.2:n.1951-233_1951-231del
XM_011514104.1:c.421-233_421-231del XP_011512406.1:n.421-233_421-231del
XM_011514105.1:c.307-233_307-231del XP_011512407.1:n.307-233_307-231del
XM_011514106.1:c.307-233_307-231del XP_011512408.1:n.307-233_307-231del
NR_149162.1:n.2009-233_2009-231del
NR_149163.1:n.2009-233_2009-231del
NM_001193376.2:c.1951-233_1951-231del NP_001180305.1:n.1951-233_1951-231del
NM_198253.3:c.1951-233_1951-231del MANE Select NP_937983.2:n.1951-233_1951-231del
NR_149162.2:n.2030-233_2030-231del
NR_149163.2:n.2030-233_2030-231del
NM_001193376.3:c.1951-233_1951-231del NP_001180305.1:n.1951-233_1951-231del
NR_149162.3:n.2030-233_2030-231del
NR_149163.3:n.2030-233_2030-231del