Canonical Allele Identifier: CA1522582261
Gene: TERT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1293355_1293356delinsTC , CM000667.2:g.1293355_1293356delinsTC GRCh38
NC_000005.9:g.1293470_1293471delinsTC , CM000667.1:g.1293470_1293471delinsTC GRCh37
NC_000005.8:g.1346470_1346471delinsTC NCBI36
NG_009265.1:g.6692_6693delinsGA , LRG_343:g.6692_6693delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000310581.10:c.1530_1531delinsGA MANE Select ENSP00000309572.5:p.Trp510=
ENST00000656021.1:c.1530_1531delinsGA ENSP00000499759.1:p.Trp510=
ENST00000310581.9:c.1530_1531delinsGA ENSP00000309572.5:p.Trp510=
ENST00000334602.10:c.1530_1531delinsGA ENSP00000334346.6:p.Trp510=
ENST00000460137.6:c.1530_1531delinsGA ENSP00000425003.1:p.Trp510=
ENST00000508104.2:c.1530_1531delinsGA ENSP00000426042.2:p.Trp510=
NM_001193376.1:c.1530_1531delinsGA NP_001180305.1:p.Trp510=
NM_198253.2:c.1530_1531delinsGA , LRG_343t1:c.1530_1531delinsGA NP_937983.2:p.Trp510=
NR_149162.1:n.1588_1589delinsGA
NR_149163.1:n.1588_1589delinsGA
NM_001193376.2:c.1530_1531delinsGA NP_001180305.1:p.Trp510=
NM_198253.3:c.1530_1531delinsGA MANE Select NP_937983.2:p.Trp510=
NR_149162.2:n.1609_1610delinsGA
NR_149163.2:n.1609_1610delinsGA
NM_001193376.3:c.1530_1531delinsGA NP_001180305.1:p.Trp510=
NR_149162.3:n.1609_1610delinsGA
NR_149163.3:n.1609_1610delinsGA