Canonical Allele Identifier: CA1522559139

Gene: TERT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1294893_1294894delinsGC , CM000667.2:g.1294893_1294894delinsGC	GRCh38
NC_000005.9:g.1295008_1295009delinsGC , CM000667.1:g.1295008_1295009delinsGC	GRCh37
NC_000005.8:g.1348008_1348009delinsGC	NCBI36
NG_009265.1:g.5154_5155delinsGC , LRG_343:g.5154_5155delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310581.10:c.96_97delinsGC MANE Select	ENSP00000309572.5:p.Gly32=
ENST00000656021.1:c.96_97delinsGC	ENSP00000499759.1:p.Gly32=
ENST00000310581.9:c.96_97delinsGC	ENSP00000309572.5:p.Gly32=
ENST00000334602.10:c.96_97delinsGC	ENSP00000334346.6:p.Gly32=
ENST00000460137.6:c.96_97delinsGC	ENSP00000425003.1:p.Gly32=
ENST00000508104.2:c.96_97delinsGC	ENSP00000426042.2:p.Gly32=
ENST00000522877.1:n.176_177delinsGC
NM_001193376.1:c.96_97delinsGC	NP_001180305.1:p.Gly32=
NM_198253.2:c.96_97delinsGC , LRG_343t1:c.96_97delinsGC	NP_937983.2:p.Gly32=
NR_149162.1:n.154_155delinsGC
NR_149163.1:n.154_155delinsGC
NM_001193376.2:c.96_97delinsGC	NP_001180305.1:p.Gly32=
NM_198253.3:c.96_97delinsGC MANE Select	NP_937983.2:p.Gly32=
NR_149162.2:n.175_176delinsGC
NR_149163.2:n.175_176delinsGC
NM_001193376.3:c.96_97delinsGC	NP_001180305.1:p.Gly32=
NR_149162.3:n.175_176delinsGC
NR_149163.3:n.175_176delinsGC