Canonical Allele Identifier: CA917398119

Gene: TERT

Linked Data

• dbSNP Id: rs1579597295

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1293969_1294002del , CM000667.2:g.1293969_1294002del	GRCh38
NC_000005.9:g.1294084_1294117del , CM000667.1:g.1294084_1294117del	GRCh37
NC_000005.8:g.1347084_1347117del	NCBI36
NG_009265.1:g.6049_6082del , LRG_343:g.6049_6082del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310581.10:c.887_920del MANE Select	ENSP00000309572.5:p.His296ProfsTer?
ENST00000656021.1:c.887_920del	ENSP00000499759.1:p.His296ProfsTer?
ENST00000310581.9:c.887_920del	ENSP00000309572.5:p.His296ProfsTer?
ENST00000334602.10:c.887_920del	ENSP00000334346.6:p.His296ProfsTer?
ENST00000460137.6:c.887_920del	ENSP00000425003.1:p.His296ProfsTer?
ENST00000508104.2:c.887_920del	ENSP00000426042.2:p.His296ProfsTer?
NM_001193376.1:c.887_920del	NP_001180305.1:p.His296ProfsTer?
NM_198253.2:c.887_920del , LRG_343t1:c.887_920del	NP_937983.2:p.His296ProfsTer?
NR_149162.1:n.945_978del
NR_149163.1:n.945_978del
NM_001193376.2:c.887_920del	NP_001180305.1:p.His296ProfsTer?
NM_198253.3:c.887_920del MANE Select	NP_937983.2:p.His296ProfsTer?
NR_149162.2:n.966_999del
NR_149163.2:n.966_999del
NM_001193376.3:c.887_920del	NP_001180305.1:p.His296ProfsTer?
NR_149162.3:n.966_999del
NR_149163.3:n.966_999del