Canonical Allele Identifier: CA1522574914

Gene: TERT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1286593G= , CM000667.2:g.1286593G=	GRCh38
NC_000005.9:g.1286708G= , CM000667.1:g.1286708G=	GRCh37
NC_000005.8:g.1339708G=	NCBI36
NG_009265.1:g.13455C= , LRG_343:g.13455C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310581.10:c.1574-3969C= MANE Select	ENSP00000309572.5:n.1574-3969C=
ENST00000656021.1:c.*691C=	ENSP00000499759.1:n.*691C=
ENST00000310581.9:c.1574-3969C=	ENSP00000309572.5:n.1574-3969C=
ENST00000334602.10:c.1574-3969C=	ENSP00000334346.6:n.1574-3969C=
ENST00000460137.6:c.1574-3969C=	ENSP00000425003.1:n.1574-3969C=
ENST00000508104.2:c.1574-3969C=	ENSP00000426042.2:n.1574-3969C=
NM_001193376.1:c.1574-3969C=	NP_001180305.1:n.1574-3969C=
NM_198253.2:c.1574-3969C= , LRG_343t1:c.1574-3969C=	NP_937983.2:n.1574-3969C=
XM_011514104.1:c.-386C=	XP_011512406.1:n.-386C=
XM_011514105.1:c.-541C=	XP_011512407.1:n.-541C=
NR_149162.1:n.1632-3969C=
NR_149163.1:n.1632-3969C=
NM_001193376.2:c.1574-3969C=	NP_001180305.1:n.1574-3969C=
NM_198253.3:c.1574-3969C= MANE Select	NP_937983.2:n.1574-3969C=
NR_149162.2:n.1653-3969C=
NR_149163.2:n.1653-3969C=
NM_001193376.3:c.1574-3969C=	NP_001180305.1:n.1574-3969C=
NR_149162.3:n.1653-3969C=
NR_149163.3:n.1653-3969C=