Canonical Allele Identifier: CA1072505606

Gene: TERT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1275746_1275781del , CM000667.2:g.1275746_1275781del	GRCh38
NC_000005.9:g.1275861_1275896del , CM000667.1:g.1275861_1275896del	GRCh37
NC_000005.8:g.1328861_1328896del	NCBI36
NG_009265.1:g.24269_24304del , LRG_343:g.24269_24304del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310581.10:c.2286+2862_2286+2897del MANE Select	ENSP00000309572.5:n.2286+2862_2286+2897del
ENST00000656021.1:c.*1832+2862_*1832+2897del	ENSP00000499759.1:n.*1832+2862_*1832+2897del
ENST00000310581.9:c.2286+2862_2286+2897del	ENSP00000309572.5:n.2286+2862_2286+2897del
ENST00000334602.10:c.2286+2862_2286+2897del	ENSP00000334346.6:n.2286+2862_2286+2897del
ENST00000460137.6:c.2250+2862_2250+2897del	ENSP00000425003.1:n.2250+2862_2250+2897del
ENST00000484238.6:n.1099+2862_1099+2897del
ENST00000508104.2:c.2286+2862_2286+2897del	ENSP00000426042.2:n.2286+2862_2286+2897del
NM_001193376.1:c.2286+2862_2286+2897del	NP_001180305.1:n.2286+2862_2286+2897del
NM_198253.2:c.2286+2862_2286+2897del , LRG_343t1:c.2286+2862_2286+2897del	NP_937983.2:n.2286+2862_2286+2897del
XM_011514104.1:c.756+2862_756+2897del	XP_011512406.1:n.756+2862_756+2897del
XM_011514105.1:c.642+2862_642+2897del	XP_011512407.1:n.642+2862_642+2897del
XM_011514106.1:c.642+2862_642+2897del	XP_011512408.1:n.642+2862_642+2897del
NR_149162.1:n.2344+2862_2344+2897del
NR_149163.1:n.2308+2862_2308+2897del
NM_001193376.2:c.2286+2862_2286+2897del	NP_001180305.1:n.2286+2862_2286+2897del
NM_198253.3:c.2286+2862_2286+2897del MANE Select	NP_937983.2:n.2286+2862_2286+2897del
NR_149162.2:n.2365+2862_2365+2897del
NR_149163.2:n.2329+2862_2329+2897del
NM_001193376.3:c.2286+2862_2286+2897del	NP_001180305.1:n.2286+2862_2286+2897del
NR_149162.3:n.2365+2862_2365+2897del
NR_149163.3:n.2329+2862_2329+2897del