Canonical Allele Identifier: CA1522565477

Gene: TERT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1279329G= , CM000667.2:g.1279329G=	GRCh38
NC_000005.9:g.1279444G= , CM000667.1:g.1279444G=	GRCh37
NC_000005.8:g.1332444G=	NCBI36
NG_009265.1:g.20719C= , LRG_343:g.20719C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310581.10:c.2092C= MANE Select	ENSP00000309572.5:p.Arg698=
ENST00000656021.1:c.*1638C=	ENSP00000499759.1:n.*1638C=
ENST00000310581.9:c.2092C=	ENSP00000309572.5:p.Arg698=
ENST00000334602.10:c.2092C=	ENSP00000334346.6:p.Arg698=
ENST00000460137.6:c.2092C=	ENSP00000425003.1:p.Arg698=
ENST00000484238.6:n.905C=
ENST00000508104.2:c.2092C=	ENSP00000426042.2:p.Arg698=
NM_001193376.1:c.2092C=	NP_001180305.1:p.Arg698=
NM_198253.2:c.2092C= , LRG_343t1:c.2092C=	NP_937983.2:p.Arg698=
XM_011514104.1:c.562C=	XP_011512406.1:p.Arg188=
XM_011514105.1:c.448C=	XP_011512407.1:p.Arg150=
XM_011514106.1:c.448C=	XP_011512408.1:p.Arg150=
NR_149162.1:n.2150C=
NR_149163.1:n.2150C=
NM_001193376.2:c.2092C=	NP_001180305.1:p.Arg698=
NM_198253.3:c.2092C= MANE Select	NP_937983.2:p.Arg698=
NR_149162.2:n.2171C=
NR_149163.2:n.2171C=
NM_001193376.3:c.2092C=	NP_001180305.1:p.Arg698=
NR_149162.3:n.2171C=
NR_149163.3:n.2171C=