Canonical Allele Identifier: CA3123422776

Gene: TERT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1278687A= , CM000667.2:g.1278687A=	GRCh38
NC_000005.9:g.1278802A= , CM000667.1:g.1278802A=	GRCh37
NC_000005.8:g.1331802A=	NCBI36
NG_009265.1:g.21361T= , LRG_343:g.21361T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310581.10:c.2240T= MANE Select	ENSP00000309572.5:p.Val747=
ENST00000656021.1:c.*1786T=	ENSP00000499759.1:n.*1786T=
ENST00000310581.9:c.2240T=	ENSP00000309572.5:p.Val747=
ENST00000334602.10:c.2240T=	ENSP00000334346.6:p.Val747=
ENST00000460137.6:c.2204T=	ENSP00000425003.1:p.Val735=
ENST00000484238.6:n.1053T=
ENST00000508104.2:c.2240T=	ENSP00000426042.2:p.Val747=
NM_001193376.1:c.2240T=	NP_001180305.1:p.Val747=
NM_198253.2:c.2240T= , LRG_343t1:c.2240T=	NP_937983.2:p.Val747=
XM_011514104.1:c.710T=	XP_011512406.1:p.Val237=
XM_011514105.1:c.596T=	XP_011512407.1:p.Val199=
XM_011514106.1:c.596T=	XP_011512408.1:p.Val199=
NR_149162.1:n.2298T=
NR_149163.1:n.2262T=
NM_001193376.2:c.2240T=	NP_001180305.1:p.Val747=
NM_198253.3:c.2240T= MANE Select	NP_937983.2:p.Val747=
NR_149162.2:n.2319T=
NR_149163.2:n.2283T=
NM_001193376.3:c.2240T=	NP_001180305.1:p.Val747=
NR_149162.3:n.2319T=
NR_149163.3:n.2283T=