Canonical Allele Identifier: CA2673079141
Gene: TERT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1272285_1272286insTTGCGGACGTGCCCATGGGCGGCCTTCT , CM000667.2:g.1272285_1272286insTTGCGGACGTGCCCATGGGCGGCCTTCT GRCh38
NC_000005.9:g.1272400_1272401insTTGCGGACGTGCCCATGGGCGGCCTTCT , CM000667.1:g.1272400_1272401insTTGCGGACGTGCCCATGGGCGGCCTTCT GRCh37
NC_000005.8:g.1325400_1325401insTTGCGGACGTGCCCATGGGCGGCCTTCT NCBI36
NG_009265.1:g.27762_27763insAGAAGGCCGCCCATGGGCACGTCCGCAA , LRG_343:g.27762_27763insAGAAGGCCGCCCATGGGCACGTCCGCAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000310581.10:c.2287-6_2287-5insAGAAGGCCGCCCATGGGCACGTCCGCAA MANE Select ENSP00000309572.5:n.2287-6_2287-5insAGAAGGCCGCCCATGGGCACGTCCG...
ENST00000656021.1:c.*1833-6_*1833-5insAGAAGGCCGCCCATGGGCACGTCCGCAA ENSP00000499759.1:n.*1833-6_*1833-5insAGAAGGCCGCCCATGGGCACGTC...
ENST00000310581.9:c.2287-6_2287-5insAGAAGGCCGCCCATGGGCACGTCCGCAA ENSP00000309572.5:n.2287-6_2287-5insAGAAGGCCGCCCATGGGCACGTCCG...
ENST00000334602.10:c.2287-6_2287-5insAGAAGGCCGCCCATGGGCACGTCCGCAA ENSP00000334346.6:n.2287-6_2287-5insAGAAGGCCGCCCATGGGCACGTCCG...
ENST00000460137.6:c.2251-3653_2251-3652insAGAAGGCCGCCCATGGGCACGTCCGCAA ENSP00000425003.1:n.2251-3653_2251-3652insAGAAGGCCGCCCATGGGCA...
ENST00000484238.6:n.1100-3653_1100-3652insAGAAGGCCGCCCATGGGCACGTCCGCAA
ENST00000508104.2:c.2287-3653_2287-3652insAGAAGGCCGCCCATGGGCACGTCCGCAA ENSP00000426042.2:n.2287-3653_2287-3652insAGAAGGCCGCCCATGGGCA...
NM_001193376.1:c.2287-6_2287-5insAGAAGGCCGCCCATGGGCACGTCCGCAA NP_001180305.1:n.2287-6_2287-5insAGAAGGCCGCCCATGGGCACGTCCGCAA...
NM_198253.2:c.2287-6_2287-5insAGAAGGCCGCCCATGGGCACGTCCGCAA , LRG_343t1:c.2287-6_2287-5insAGAAGGCCGCCCATGGGCACGTCCGCAA NP_937983.2:n.2287-6_2287-5insAGAAGGCCGCCCATGGGCACGTCCGCAA
XM_011514104.1:c.757-6_757-5insAGAAGGCCGCCCATGGGCACGTCCGCAA XP_011512406.1:n.757-6_757-5insAGAAGGCCGCCCATGGGCACGTCCGCAA
XM_011514105.1:c.643-6_643-5insAGAAGGCCGCCCATGGGCACGTCCGCAA XP_011512407.1:n.643-6_643-5insAGAAGGCCGCCCATGGGCACGTCCGCAA
XM_011514106.1:c.643-6_643-5insAGAAGGCCGCCCATGGGCACGTCCGCAA XP_011512408.1:n.643-6_643-5insAGAAGGCCGCCCATGGGCACGTCCGCAA
NR_149162.1:n.2345-3653_2345-3652insAGAAGGCCGCCCATGGGCACGTCCGCAA
NR_149163.1:n.2309-3653_2309-3652insAGAAGGCCGCCCATGGGCACGTCCGCAA
NM_001193376.2:c.2287-6_2287-5insAGAAGGCCGCCCATGGGCACGTCCGCAA NP_001180305.1:n.2287-6_2287-5insAGAAGGCCGCCCATGGGCACGTCCGCAA...
NM_198253.3:c.2287-6_2287-5insAGAAGGCCGCCCATGGGCACGTCCGCAA MANE Select NP_937983.2:n.2287-6_2287-5insAGAAGGCCGCCCATGGGCACGTCCGCAA
NR_149162.2:n.2366-3653_2366-3652insAGAAGGCCGCCCATGGGCACGTCCGCAA
NR_149163.2:n.2330-3653_2330-3652insAGAAGGCCGCCCATGGGCACGTCCGCAA
NM_001193376.3:c.2287-6_2287-5insAGAAGGCCGCCCATGGGCACGTCCGCAA NP_001180305.1:n.2287-6_2287-5insAGAAGGCCGCCCATGGGCACGTCCGCAA...
NR_149162.3:n.2366-3653_2366-3652insAGAAGGCCGCCCATGGGCACGTCCGCAA
NR_149163.3:n.2330-3653_2330-3652insAGAAGGCCGCCCATGGGCACGTCCGCAA