Canonical Allele Identifier: CA2673078934

Gene: TERT

Linked Data

• gnomAD v4: 5-1272045-CTCA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1272050_1272052del , CM000667.2:g.1272050_1272052del	GRCh38
NC_000005.9:g.1272165_1272167del , CM000667.1:g.1272165_1272167del	GRCh37
NC_000005.8:g.1325165_1325167del	NCBI36
NG_009265.1:g.28000_28002del , LRG_343:g.28000_28002del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310581.10:c.2382+137_2382+139del MANE Select	ENSP00000309572.5:n.2382+137_2382+139del
ENST00000656021.1:c.*1928+137_*1928+139del	ENSP00000499759.1:n.*1928+137_*1928+139del
ENST00000310581.9:c.2382+137_2382+139del	ENSP00000309572.5:n.2382+137_2382+139del
ENST00000334602.10:c.2382+137_2382+139del	ENSP00000334346.6:n.2382+137_2382+139del
ENST00000460137.6:c.2251-3415_2251-3413del	ENSP00000425003.1:n.2251-3415_2251-3413del
ENST00000484238.6:n.1100-3415_1100-3413del
ENST00000508104.2:c.2287-3415_2287-3413del	ENSP00000426042.2:n.2287-3415_2287-3413del
NM_001193376.1:c.2382+137_2382+139del	NP_001180305.1:n.2382+137_2382+139del
NM_198253.2:c.2382+137_2382+139del , LRG_343t1:c.2382+137_2382+139del	NP_937983.2:n.2382+137_2382+139del
XM_011514104.1:c.852+137_852+139del	XP_011512406.1:n.852+137_852+139del
XM_011514105.1:c.738+137_738+139del	XP_011512407.1:n.738+137_738+139del
XM_011514106.1:c.738+137_738+139del	XP_011512408.1:n.738+137_738+139del
NR_149162.1:n.2345-3415_2345-3413del
NR_149163.1:n.2309-3415_2309-3413del
NM_001193376.2:c.2382+137_2382+139del	NP_001180305.1:n.2382+137_2382+139del
NM_198253.3:c.2382+137_2382+139del MANE Select	NP_937983.2:n.2382+137_2382+139del
NR_149162.2:n.2366-3415_2366-3413del
NR_149163.2:n.2330-3415_2330-3413del
NM_001193376.3:c.2382+137_2382+139del	NP_001180305.1:n.2382+137_2382+139del
NR_149162.3:n.2366-3415_2366-3413del
NR_149163.3:n.2330-3415_2330-3413del