Canonical Allele Identifier: CA1522545705

Gene: TERT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1266524C= , CM000667.2:g.1266524C=	GRCh38
NC_000005.9:g.1266639C= , CM000667.1:g.1266639C=	GRCh37
NC_000005.8:g.1319639C=	NCBI36
NG_009265.1:g.33524G= , LRG_343:g.33524G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310581.10:c.2594G= MANE Select	ENSP00000309572.5:p.Arg865=
ENST00000656021.1:c.*2140G=	ENSP00000499759.1:n.*2140G=
ENST00000310581.9:c.2594G=	ENSP00000309572.5:p.Arg865=
ENST00000334602.10:c.2594G=	ENSP00000334346.6:p.Arg865=
ENST00000460137.6:c.2376G=	ENSP00000425003.1:p.Ala792=
ENST00000484238.6:n.1225G=
ENST00000503656.1:n.1G=
ENST00000508104.2:c.2412G=	ENSP00000426042.2:p.Ala804=
NM_001193376.1:c.2594G=	NP_001180305.1:p.Arg865=
NM_198253.2:c.2594G= , LRG_343t1:c.2594G=	NP_937983.2:p.Arg865=
XM_011514104.1:c.1064G=	XP_011512406.1:p.Arg355=
XM_011514105.1:c.950G=	XP_011512407.1:p.Arg317=
XM_011514106.1:c.950G=	XP_011512408.1:p.Arg317=
NR_149162.1:n.2470G=
NR_149163.1:n.2434G=
NM_001193376.2:c.2594G=	NP_001180305.1:p.Arg865=
NM_198253.3:c.2594G= MANE Select	NP_937983.2:p.Arg865=
NR_149162.2:n.2491G=
NR_149163.2:n.2455G=
NM_001193376.3:c.2594G=	NP_001180305.1:p.Arg865=
NR_149162.3:n.2491G=
NR_149163.3:n.2455G=