Canonical Allele Identifier: CA2673077804
Gene: TERT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1266536_1266537insCGTCCCGCCGAATCCCCGCAAACAGCTTGTTCTCCA , CM000667.2:g.1266536_1266537insCGTCCCGCCGAATCCCCGCAAACAGCTTGTTCTCCA GRCh38
NC_000005.9:g.1266651_1266652insCGTCCCGCCGAATCCCCGCAAACAGCTTGTTCTCCA , CM000667.1:g.1266651_1266652insCGTCCCGCCGAATCCCCGCAAACAGCTTGTTCTCCA GRCh37
NC_000005.8:g.1319651_1319652insCGTCCCGCCGAATCCCCGCAAACAGCTTGTTCTCCA NCBI36
NG_009265.1:g.33511_33512insTGGAGAACAAGCTGTTTGCGGGGATTCGGCGGGACG , LRG_343:g.33511_33512insTGGAGAACAAGCTGTTTGCGGGGATTCGGCGGGACG

Transcript Alleles

HGVS Amino-acid Change
ENST00000310581.10:c.2583-2_2583-1insTGGAGAACAAGCTGTTTGCGGGGATTCGGCGGGACG MANE Select ENSP00000309572.5:n.2583-2_2583-1insTGGAGAACAAGCTGTTTGCGGGGAT...
ENST00000656021.1:c.*2129-2_*2129-1insTGGAGAACAAGCTGTTTGCGGGGATTCGGCGGGACG ENSP00000499759.1:n.*2129-2_*2129-1insTGGAGAACAAGCTGTTTGCGGGG...
ENST00000310581.9:c.2583-2_2583-1insTGGAGAACAAGCTGTTTGCGGGGATTCGGCGGGACG ENSP00000309572.5:n.2583-2_2583-1insTGGAGAACAAGCTGTTTGCGGGGAT...
ENST00000334602.10:c.2583-2_2583-1insTGGAGAACAAGCTGTTTGCGGGGATTCGGCGGGACG ENSP00000334346.6:n.2583-2_2583-1insTGGAGAACAAGCTGTTTGCGGGGAT...
ENST00000460137.6:c.2365-2_2365-1insTGGAGAACAAGCTGTTTGCGGGGATTCGGCGGGACG ENSP00000425003.1:n.2365-2_2365-1insTGGAGAACAAGCTGTTTGCGGGGAT...
ENST00000484238.6:n.1214-2_1214-1insTGGAGAACAAGCTGTTTGCGGGGATTCGGCGGGACG
ENST00000508104.2:c.2401-2_2401-1insTGGAGAACAAGCTGTTTGCGGGGATTCGGCGGGACG ENSP00000426042.2:n.2401-2_2401-1insTGGAGAACAAGCTGTTTGCGGGGAT...
NM_001193376.1:c.2583-2_2583-1insTGGAGAACAAGCTGTTTGCGGGGATTCGGCGGGACG NP_001180305.1:n.2583-2_2583-1insTGGAGAACAAGCTGTTTGCGGGGATTCG...
NM_198253.2:c.2583-2_2583-1insTGGAGAACAAGCTGTTTGCGGGGATTCGGCGGGACG , LRG_343t1:c.2583-2_2583-1insTGGAGAACAAGCTGTTTGCGGGGATTCGGCGGGACG NP_937983.2:n.2583-2_2583-1insTGGAGAACAAGCTGTTTGCGGGGATTCGGCG...
XM_011514104.1:c.1053-2_1053-1insTGGAGAACAAGCTGTTTGCGGGGATTCGGCGGGACG XP_011512406.1:n.1053-2_1053-1insTGGAGAACAAGCTGTTTGCGGGGATTCG...
XM_011514105.1:c.939-2_939-1insTGGAGAACAAGCTGTTTGCGGGGATTCGGCGGGACG XP_011512407.1:n.939-2_939-1insTGGAGAACAAGCTGTTTGCGGGGATTCGGC...
XM_011514106.1:c.939-2_939-1insTGGAGAACAAGCTGTTTGCGGGGATTCGGCGGGACG XP_011512408.1:n.939-2_939-1insTGGAGAACAAGCTGTTTGCGGGGATTCGGC...
NR_149162.1:n.2459-2_2459-1insTGGAGAACAAGCTGTTTGCGGGGATTCGGCGGGACG
NR_149163.1:n.2423-2_2423-1insTGGAGAACAAGCTGTTTGCGGGGATTCGGCGGGACG
NM_001193376.2:c.2583-2_2583-1insTGGAGAACAAGCTGTTTGCGGGGATTCGGCGGGACG NP_001180305.1:n.2583-2_2583-1insTGGAGAACAAGCTGTTTGCGGGGATTCG...
NM_198253.3:c.2583-2_2583-1insTGGAGAACAAGCTGTTTGCGGGGATTCGGCGGGACG MANE Select NP_937983.2:n.2583-2_2583-1insTGGAGAACAAGCTGTTTGCGGGGATTCGGCG...
NR_149162.2:n.2480-2_2480-1insTGGAGAACAAGCTGTTTGCGGGGATTCGGCGGGACG
NR_149163.2:n.2444-2_2444-1insTGGAGAACAAGCTGTTTGCGGGGATTCGGCGGGACG
NM_001193376.3:c.2583-2_2583-1insTGGAGAACAAGCTGTTTGCGGGGATTCGGCGGGACG NP_001180305.1:n.2583-2_2583-1insTGGAGAACAAGCTGTTTGCGGGGATTCG...
NR_149162.3:n.2480-2_2480-1insTGGAGAACAAGCTGTTTGCGGGGATTCGGCGGGACG
NR_149163.3:n.2444-2_2444-1insTGGAGAACAAGCTGTTTGCGGGGATTCGGCGGGACG