Canonical Allele Identifier: CA1522545646

Gene: TERT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1266487G= , CM000667.2:g.1266487G=	GRCh38
NC_000005.9:g.1266602G= , CM000667.1:g.1266602G=	GRCh37
NC_000005.8:g.1319602G=	NCBI36
NG_009265.1:g.33561C= , LRG_343:g.33561C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310581.10:c.2631C= MANE Select	ENSP00000309572.5:p.Leu877=
ENST00000656021.1:c.*2177C=	ENSP00000499759.1:n.*2177C=
ENST00000310581.9:c.2631C=	ENSP00000309572.5:p.Leu877=
ENST00000334602.10:c.2631C=	ENSP00000334346.6:p.Leu877=
ENST00000460137.6:c.2413C=	ENSP00000425003.1:n.2413C=
ENST00000484238.6:n.1262C=
ENST00000503656.1:n.38C=
ENST00000508104.2:c.2449C=	ENSP00000426042.2:n.2449C=
NM_001193376.1:c.2631C=	NP_001180305.1:p.Leu877=
NM_198253.2:c.2631C= , LRG_343t1:c.2631C=	NP_937983.2:p.Leu877=
XM_011514104.1:c.1101C=	XP_011512406.1:p.Leu367=
XM_011514105.1:c.987C=	XP_011512407.1:p.Leu329=
XM_011514106.1:c.987C=	XP_011512408.1:p.Leu329=
NR_149162.1:n.2507C=
NR_149163.1:n.2471C=
NM_001193376.2:c.2631C=	NP_001180305.1:p.Leu877=
NM_198253.3:c.2631C= MANE Select	NP_937983.2:p.Leu877=
NR_149162.2:n.2528C=
NR_149163.2:n.2492C=
NM_001193376.3:c.2631C=	NP_001180305.1:p.Leu877=
NR_149162.3:n.2528C=
NR_149163.3:n.2492C=