Canonical Allele Identifier: CA1522564445

Gene: TERT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1278656C= , CM000667.2:g.1278656C=	GRCh38
NC_000005.9:g.1278771C= , CM000667.1:g.1278771C=	GRCh37
NC_000005.8:g.1331771C=	NCBI36
NG_009265.1:g.21392G= , LRG_343:g.21392G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000310581.10:c.2271G= MANE Select	ENSP00000309572.5:p.Lys757=
ENST00000656021.1:c.*1817G=	ENSP00000499759.1:n.*1817G=
ENST00000310581.9:c.2271G=	ENSP00000309572.5:p.Lys757=
ENST00000334602.10:c.2271G=	ENSP00000334346.6:p.Lys757=
ENST00000460137.6:c.2235G=	ENSP00000425003.1:p.Lys745=
ENST00000484238.6:n.1084G=
ENST00000508104.2:c.2271G=	ENSP00000426042.2:p.Lys757=
NM_001193376.1:c.2271G=	NP_001180305.1:p.Lys757=
NM_198253.2:c.2271G= , LRG_343t1:c.2271G=	NP_937983.2:p.Lys757=
XM_011514104.1:c.741G=	XP_011512406.1:p.Lys247=
XM_011514105.1:c.627G=	XP_011512407.1:p.Lys209=
XM_011514106.1:c.627G=	XP_011512408.1:p.Lys209=
NR_149162.1:n.2329G=
NR_149163.1:n.2293G=
NM_001193376.2:c.2271G=	NP_001180305.1:p.Lys757=
NM_198253.3:c.2271G= MANE Select	NP_937983.2:p.Lys757=
NR_149162.2:n.2350G=
NR_149163.2:n.2314G=
NM_001193376.3:c.2271G=	NP_001180305.1:p.Lys757=
NR_149162.3:n.2350G=
NR_149163.3:n.2314G=