Canonical Allele Identifier: CA1522574790

Gene: TERT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1286453G= , CM000667.2:g.1286453G=	GRCh38
NC_000005.9:g.1286568G= , CM000667.1:g.1286568G=	GRCh37
NC_000005.8:g.1339568G=	NCBI36
NG_009265.1:g.13595C= , LRG_343:g.13595C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310581.10:c.1574-3829C= MANE Select	ENSP00000309572.5:n.1574-3829C=
ENST00000656021.1:c.*831C=	ENSP00000499759.1:n.*831C=
ENST00000310581.9:c.1574-3829C=	ENSP00000309572.5:n.1574-3829C=
ENST00000334602.10:c.1574-3829C=	ENSP00000334346.6:n.1574-3829C=
ENST00000460137.6:c.1574-3829C=	ENSP00000425003.1:n.1574-3829C=
ENST00000508104.2:c.1574-3829C=	ENSP00000426042.2:n.1574-3829C=
NM_001193376.1:c.1574-3829C=	NP_001180305.1:n.1574-3829C=
NM_198253.2:c.1574-3829C= , LRG_343t1:c.1574-3829C=	NP_937983.2:n.1574-3829C=
XM_011514104.1:c.-246C=	XP_011512406.1:n.-246C=
XM_011514105.1:c.-401C=	XP_011512407.1:n.-401C=
NR_149162.1:n.1632-3829C=
NR_149163.1:n.1632-3829C=
NM_001193376.2:c.1574-3829C=	NP_001180305.1:n.1574-3829C=
NM_198253.3:c.1574-3829C= MANE Select	NP_937983.2:n.1574-3829C=
NR_149162.2:n.1653-3829C=
NR_149163.2:n.1653-3829C=
NM_001193376.3:c.1574-3829C=	NP_001180305.1:n.1574-3829C=
NR_149162.3:n.1653-3829C=
NR_149163.3:n.1653-3829C=