Canonical Allele Identifier: CA1522539783

Gene: TERT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1260488A= , CM000667.2:g.1260488A=	GRCh38
NC_000005.9:g.1260603A= , CM000667.1:g.1260603A=	GRCh37
NC_000005.8:g.1313603A=	NCBI36
NG_009265.1:g.39560T= , LRG_343:g.39560T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310581.10:c.2956T= MANE Select	ENSP00000309572.5:p.Phe986=
ENST00000656021.1:c.*2502T=	ENSP00000499759.1:n.*2502T=
ENST00000667927.1:n.244T=
ENST00000310581.9:c.2956T=	ENSP00000309572.5:p.Phe986=
ENST00000334602.10:c.2767T=	ENSP00000334346.6:p.Phe923=
ENST00000460137.6:c.2549T=	ENSP00000425003.1:n.2549T=
ENST00000484238.6:n.1398T=
NM_001193376.1:c.2767T=	NP_001180305.1:p.Phe923=
NM_198253.2:c.2956T= , LRG_343t1:c.2956T=	NP_937983.2:p.Phe986=
XM_011514104.1:c.1426T=	XP_011512406.1:p.Phe476=
XM_011514105.1:c.1312T=	XP_011512407.1:p.Phe438=
XM_011514106.1:c.1312T=	XP_011512408.1:p.Phe438=
NR_149162.1:n.2643T=
NR_149163.1:n.2607T=
NM_001193376.2:c.2767T=	NP_001180305.1:p.Phe923=
NM_198253.3:c.2956T= MANE Select	NP_937983.2:p.Phe986=
NR_149162.2:n.2664T=
NR_149163.2:n.2628T=
NM_001193376.3:c.2767T=	NP_001180305.1:p.Phe923=
NR_149162.3:n.2664T=
NR_149163.3:n.2628T=