Canonical Allele Identifier: CA1522564479

Gene: TERT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1278672T= , CM000667.2:g.1278672T=	GRCh38
NC_000005.9:g.1278787T= , CM000667.1:g.1278787T=	GRCh37
NC_000005.8:g.1331787T=	NCBI36
NG_009265.1:g.21376A= , LRG_343:g.21376A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000310581.10:c.2255A= MANE Select	ENSP00000309572.5:p.His752=
ENST00000656021.1:c.*1801A=	ENSP00000499759.1:n.*1801A=
ENST00000310581.9:c.2255A=	ENSP00000309572.5:p.His752=
ENST00000334602.10:c.2255A=	ENSP00000334346.6:p.His752=
ENST00000460137.6:c.2219A=	ENSP00000425003.1:p.His740=
ENST00000484238.6:n.1068A=
ENST00000508104.2:c.2255A=	ENSP00000426042.2:p.His752=
NM_001193376.1:c.2255A=	NP_001180305.1:p.His752=
NM_198253.2:c.2255A= , LRG_343t1:c.2255A=	NP_937983.2:p.His752=
XM_011514104.1:c.725A=	XP_011512406.1:p.His242=
XM_011514105.1:c.611A=	XP_011512407.1:p.His204=
XM_011514106.1:c.611A=	XP_011512408.1:p.His204=
NR_149162.1:n.2313A=
NR_149163.1:n.2277A=
NM_001193376.2:c.2255A=	NP_001180305.1:p.His752=
NM_198253.3:c.2255A= MANE Select	NP_937983.2:p.His752=
NR_149162.2:n.2334A=
NR_149163.2:n.2298A=
NM_001193376.3:c.2255A=	NP_001180305.1:p.His752=
NR_149162.3:n.2334A=
NR_149163.3:n.2298A=