Canonical Allele Identifier: CA1072495893
Gene: TERT HGNC NCBI

Linked Data

dbSNP Id: rs1748137585

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1260394_1260395del , CM000667.2:g.1260394_1260395del GRCh38
NC_000005.9:g.1260509_1260510del , CM000667.1:g.1260509_1260510del GRCh37
NC_000005.8:g.1313509_1313510del NCBI36
NG_009265.1:g.39654_39655del , LRG_343:g.39654_39655del

Transcript Alleles

HGVS Amino-acid change
ENST00000310581.10:c.2970+80_2970+81del MANE Select ENSP00000309572.5:n.2970+80_2970+81del
ENST00000656021.1:c.*2516+80_*2516+81del ENSP00000499759.1:n.*2516+80_*2516+81del
ENST00000667927.1:n.258+80_258+81del
ENST00000310581.9:c.2970+80_2970+81del ENSP00000309572.5:n.2970+80_2970+81del
ENST00000334602.10:c.2781+80_2781+81del ENSP00000334346.6:n.2781+80_2781+81del
ENST00000460137.6:c.2563+80_2563+81del ENSP00000425003.1:n.2563+80_2563+81del
ENST00000484238.6:n.1412+80_1412+81del
NM_001193376.1:c.2781+80_2781+81del NP_001180305.1:n.2781+80_2781+81del
NM_198253.2:c.2970+80_2970+81del , LRG_343t1:c.2970+80_2970+81del NP_937983.2:n.2970+80_2970+81del
XM_011514104.1:c.1440+80_1440+81del XP_011512406.1:n.1440+80_1440+81del
XM_011514105.1:c.1326+80_1326+81del XP_011512407.1:n.1326+80_1326+81del
XM_011514106.1:c.1326+80_1326+81del XP_011512408.1:n.1326+80_1326+81del
NR_149162.1:n.2657+80_2657+81del
NR_149163.1:n.2621+80_2621+81del
NM_001193376.2:c.2781+80_2781+81del NP_001180305.1:n.2781+80_2781+81del
NM_198253.3:c.2970+80_2970+81del MANE Select NP_937983.2:n.2970+80_2970+81del
NR_149162.2:n.2678+80_2678+81del
NR_149163.2:n.2642+80_2642+81del
NM_001193376.3:c.2781+80_2781+81del NP_001180305.1:n.2781+80_2781+81del
NR_149162.3:n.2678+80_2678+81del
NR_149163.3:n.2642+80_2642+81del