Canonical Allele Identifier: CA2673080547
Gene: TERT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1293191_1293192del , CM000667.2:g.1293191_1293192del GRCh38
NC_000005.9:g.1293306_1293307del , CM000667.1:g.1293306_1293307del GRCh37
NC_000005.8:g.1346306_1346307del NCBI36
NG_009265.1:g.6858_6859del , LRG_343:g.6858_6859del

Transcript Alleles

HGVS Amino-acid Change
ENST00000310581.10:c.1573+123_1573+124del MANE Select ENSP00000309572.5:n.1573+123_1573+124del
ENST00000656021.1:c.1696_1697del ENSP00000499759.1:p.Phe566ArgfsTer22
ENST00000310581.9:c.1573+123_1573+124del ENSP00000309572.5:n.1573+123_1573+124del
ENST00000334602.10:c.1573+123_1573+124del ENSP00000334346.6:n.1573+123_1573+124del
ENST00000460137.6:c.1573+123_1573+124del ENSP00000425003.1:n.1573+123_1573+124del
ENST00000508104.2:c.1573+123_1573+124del ENSP00000426042.2:n.1573+123_1573+124del
NM_001193376.1:c.1573+123_1573+124del NP_001180305.1:n.1573+123_1573+124del
NM_198253.2:c.1573+123_1573+124del , LRG_343t1:c.1573+123_1573+124del NP_937983.2:n.1573+123_1573+124del
NR_149162.1:n.1631+123_1631+124del
NR_149163.1:n.1631+123_1631+124del
NM_001193376.2:c.1573+123_1573+124del NP_001180305.1:n.1573+123_1573+124del
NM_198253.3:c.1573+123_1573+124del MANE Select NP_937983.2:n.1573+123_1573+124del
NR_149162.2:n.1652+123_1652+124del
NR_149163.2:n.1652+123_1652+124del
NM_001193376.3:c.1573+123_1573+124del NP_001180305.1:n.1573+123_1573+124del
NR_149162.3:n.1652+123_1652+124del
NR_149163.3:n.1652+123_1652+124del