Canonical Allele Identifier: CA1522545670

Gene: TERT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1266504A= , CM000667.2:g.1266504A=	GRCh38
NC_000005.9:g.1266619A= , CM000667.1:g.1266619A=	GRCh37
NC_000005.8:g.1319619A=	NCBI36
NG_009265.1:g.33544T= , LRG_343:g.33544T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000310581.10:c.2614T= MANE Select	ENSP00000309572.5:p.Leu872=
ENST00000656021.1:c.*2160T=	ENSP00000499759.1:n.*2160T=
ENST00000310581.9:c.2614T=	ENSP00000309572.5:p.Leu872=
ENST00000334602.10:c.2614T=	ENSP00000334346.6:p.Leu872=
ENST00000460137.6:c.2396T=	ENSP00000425003.1:n.2396T=
ENST00000484238.6:n.1245T=
ENST00000503656.1:n.21T=
ENST00000508104.2:c.2432T=	ENSP00000426042.2:n.2432T=
NM_001193376.1:c.2614T=	NP_001180305.1:p.Leu872=
NM_198253.2:c.2614T= , LRG_343t1:c.2614T=	NP_937983.2:p.Leu872=
XM_011514104.1:c.1084T=	XP_011512406.1:p.Leu362=
XM_011514105.1:c.970T=	XP_011512407.1:p.Leu324=
XM_011514106.1:c.970T=	XP_011512408.1:p.Leu324=
NR_149162.1:n.2490T=
NR_149163.1:n.2454T=
NM_001193376.2:c.2614T=	NP_001180305.1:p.Leu872=
NM_198253.3:c.2614T= MANE Select	NP_937983.2:p.Leu872=
NR_149162.2:n.2511T=
NR_149163.2:n.2475T=
NM_001193376.3:c.2614T=	NP_001180305.1:p.Leu872=
NR_149162.3:n.2511T=
NR_149163.3:n.2475T=