Canonical Allele Identifier: CA1522545717

Gene: TERT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1266526C= , CM000667.2:g.1266526C=	GRCh38
NC_000005.9:g.1266641C= , CM000667.1:g.1266641C=	GRCh37
NC_000005.8:g.1319641C=	NCBI36
NG_009265.1:g.33522G= , LRG_343:g.33522G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310581.10:c.2592G= MANE Select	ENSP00000309572.5:p.Leu864=
ENST00000656021.1:c.*2138G=	ENSP00000499759.1:n.*2138G=
ENST00000310581.9:c.2592G=	ENSP00000309572.5:p.Leu864=
ENST00000334602.10:c.2592G=	ENSP00000334346.6:p.Leu864=
ENST00000460137.6:c.2374G=	ENSP00000425003.1:p.Ala792=
ENST00000484238.6:n.1223G=
ENST00000508104.2:c.2410G=	ENSP00000426042.2:p.Ala804=
NM_001193376.1:c.2592G=	NP_001180305.1:p.Leu864=
NM_198253.2:c.2592G= , LRG_343t1:c.2592G=	NP_937983.2:p.Leu864=
XM_011514104.1:c.1062G=	XP_011512406.1:p.Leu354=
XM_011514105.1:c.948G=	XP_011512407.1:p.Leu316=
XM_011514106.1:c.948G=	XP_011512408.1:p.Leu316=
NR_149162.1:n.2468G=
NR_149163.1:n.2432G=
NM_001193376.2:c.2592G=	NP_001180305.1:p.Leu864=
NM_198253.3:c.2592G= MANE Select	NP_937983.2:p.Leu864=
NR_149162.2:n.2489G=
NR_149163.2:n.2453G=
NM_001193376.3:c.2592G=	NP_001180305.1:p.Leu864=
NR_149162.3:n.2489G=
NR_149163.3:n.2453G=