Canonical Allele Identifier: CA1522574379

Gene: TERT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1286093C= , CM000667.2:g.1286093C=	GRCh38
NC_000005.9:g.1286208C= , CM000667.1:g.1286208C=	GRCh37
NC_000005.8:g.1339208C=	NCBI36
NG_009265.1:g.13955G= , LRG_343:g.13955G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310581.10:c.1574-3469G= MANE Select	ENSP00000309572.5:n.1574-3469G=
ENST00000656021.1:c.*1119+72G=	ENSP00000499759.1:n.*1119+72G=
ENST00000310581.9:c.1574-3469G=	ENSP00000309572.5:n.1574-3469G=
ENST00000334602.10:c.1574-3469G=	ENSP00000334346.6:n.1574-3469G=
ENST00000460137.6:c.1574-3469G=	ENSP00000425003.1:n.1574-3469G=
ENST00000508104.2:c.1574-3469G=	ENSP00000426042.2:n.1574-3469G=
NM_001193376.1:c.1574-3469G=	NP_001180305.1:n.1574-3469G=
NM_198253.2:c.1574-3469G= , LRG_343t1:c.1574-3469G=	NP_937983.2:n.1574-3469G=
XM_011514104.1:c.43+72G=	XP_011512406.1:n.43+72G=
XM_011514105.1:c.-72+31G=	XP_011512407.1:n.-72+31G=
XM_011514106.1:c.-266G=	XP_011512408.1:n.-266G=
NR_149162.1:n.1632-3469G=
NR_149163.1:n.1632-3469G=
NM_001193376.2:c.1574-3469G=	NP_001180305.1:n.1574-3469G=
NM_198253.3:c.1574-3469G= MANE Select	NP_937983.2:n.1574-3469G=
NR_149162.2:n.1653-3469G=
NR_149163.2:n.1653-3469G=
NM_001193376.3:c.1574-3469G=	NP_001180305.1:n.1574-3469G=
NR_149162.3:n.1653-3469G=
NR_149163.3:n.1653-3469G=