Canonical Allele Identifier: CA1522559939

Gene: TERT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1275233G= , CM000667.2:g.1275233G=	GRCh38
NC_000005.9:g.1275348G= , CM000667.1:g.1275348G=	GRCh37
NC_000005.8:g.1328348G=	NCBI36
NG_009265.1:g.24815C= , LRG_343:g.24815C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310581.10:c.2287-2953C= MANE Select	ENSP00000309572.5:n.2287-2953C=
ENST00000656021.1:c.*1833-2953C=	ENSP00000499759.1:n.*1833-2953C=
ENST00000310581.9:c.2287-2953C=	ENSP00000309572.5:n.2287-2953C=
ENST00000334602.10:c.2287-2953C=	ENSP00000334346.6:n.2287-2953C=
ENST00000460137.6:c.2250+3408C=	ENSP00000425003.1:n.2250+3408C=
ENST00000484238.6:n.1099+3408C=
ENST00000508104.2:c.2286+3408C=	ENSP00000426042.2:n.2286+3408C=
NM_001193376.1:c.2287-2953C=	NP_001180305.1:n.2287-2953C=
NM_198253.2:c.2287-2953C= , LRG_343t1:c.2287-2953C=	NP_937983.2:n.2287-2953C=
XM_011514104.1:c.757-2953C=	XP_011512406.1:n.757-2953C=
XM_011514105.1:c.643-2953C=	XP_011512407.1:n.643-2953C=
XM_011514106.1:c.643-2953C=	XP_011512408.1:n.643-2953C=
NR_149162.1:n.2344+3408C=
NR_149163.1:n.2308+3408C=
NM_001193376.2:c.2287-2953C=	NP_001180305.1:n.2287-2953C=
NM_198253.3:c.2287-2953C= MANE Select	NP_937983.2:n.2287-2953C=
NR_149162.2:n.2365+3408C=
NR_149163.2:n.2329+3408C=
NM_001193376.3:c.2287-2953C=	NP_001180305.1:n.2287-2953C=
NR_149162.3:n.2365+3408C=
NR_149163.3:n.2329+3408C=