Canonical Allele Identifier: CA1522574606
Gene: TERT HGNC NCBI

Linked Data

dbSNP Id: rs1750480223

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1286302_1286304del , CM000667.2:g.1286302_1286304del GRCh38
NC_000005.9:g.1286417_1286419del , CM000667.1:g.1286417_1286419del GRCh37
NC_000005.8:g.1339417_1339419del NCBI36
NG_009265.1:g.13748_13750del , LRG_343:g.13748_13750del

Transcript Alleles

HGVS Amino-acid change
ENST00000310581.10:c.1574-3676_1574-3674del MANE Select ENSP00000309572.5:n.1574-3676_1574-3674de...
ENST00000656021.1:c.*984_*986del ENSP00000499759.1:n.*984_*986del
ENST00000310581.9:c.1574-3676_1574-3674del ENSP00000309572.5:n.1574-3676_1574-3674de...
ENST00000334602.10:c.1574-3676_1574-3674del ENSP00000334346.6:n.1574-3676_1574-3674de...
ENST00000460137.6:c.1574-3676_1574-3674del ENSP00000425003.1:n.1574-3676_1574-3674de...
ENST00000508104.2:c.1574-3676_1574-3674del ENSP00000426042.2:n.1574-3676_1574-3674de...
NM_001193376.1:c.1574-3676_1574-3674del NP_001180305.1:n.1574-3676_1574-3674del
NM_198253.2:c.1574-3676_1574-3674del , LRG_343t1:c.1574-3676_1574-3674del NP_937983.2:n.1574-3676_1574-3674del
XM_011514104.1:c.-93_-91del XP_011512406.1:n.-93_-91del
XM_011514105.1:c.-248_-246del XP_011512407.1:n.-248_-246del
NR_149162.1:n.1632-3676_1632-3674del
NR_149163.1:n.1632-3676_1632-3674del
NM_001193376.2:c.1574-3676_1574-3674del NP_001180305.1:n.1574-3676_1574-3674del
NM_198253.3:c.1574-3676_1574-3674del MANE Select NP_937983.2:n.1574-3676_1574-3674del
NR_149162.2:n.1653-3676_1653-3674del
NR_149163.2:n.1653-3676_1653-3674del
NM_001193376.3:c.1574-3676_1574-3674del NP_001180305.1:n.1574-3676_1574-3674del
NR_149162.3:n.1653-3676_1653-3674del
NR_149163.3:n.1653-3676_1653-3674del