Canonical Allele Identifier: CA1522555080

Gene: TERT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1293499C= , CM000667.2:g.1293499C=	GRCh38
NC_000005.9:g.1293614C= , CM000667.1:g.1293614C=	GRCh37
NC_000005.8:g.1346614C=	NCBI36
NG_009265.1:g.6549G= , LRG_343:g.6549G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310581.10:c.1387G= MANE Select	ENSP00000309572.5:p.Gly463=
ENST00000656021.1:c.1387G=	ENSP00000499759.1:p.Gly463=
ENST00000310581.9:c.1387G=	ENSP00000309572.5:p.Gly463=
ENST00000334602.10:c.1387G=	ENSP00000334346.6:p.Gly463=
ENST00000460137.6:c.1387G=	ENSP00000425003.1:p.Gly463=
ENST00000508104.2:c.1387G=	ENSP00000426042.2:p.Gly463=
NM_001193376.1:c.1387G=	NP_001180305.1:p.Gly463=
NM_198253.2:c.1387G= , LRG_343t1:c.1387G=	NP_937983.2:p.Gly463=
NR_149162.1:n.1445G=
NR_149163.1:n.1445G=
NM_001193376.2:c.1387G=	NP_001180305.1:p.Gly463=
NM_198253.3:c.1387G= MANE Select	NP_937983.2:p.Gly463=
NR_149162.2:n.1466G=
NR_149163.2:n.1466G=
NM_001193376.3:c.1387G=	NP_001180305.1:p.Gly463=
NR_149162.3:n.1466G=
NR_149163.3:n.1466G=