Canonical Allele Identifier: CA1522564448

Gene: TERT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1278657T= , CM000667.2:g.1278657T=	GRCh38
NC_000005.9:g.1278772T= , CM000667.1:g.1278772T=	GRCh37
NC_000005.8:g.1331772T=	NCBI36
NG_009265.1:g.21391A= , LRG_343:g.21391A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000310581.10:c.2270A= MANE Select	ENSP00000309572.5:p.Lys757=
ENST00000656021.1:c.*1816A=	ENSP00000499759.1:n.*1816A=
ENST00000310581.9:c.2270A=	ENSP00000309572.5:p.Lys757=
ENST00000334602.10:c.2270A=	ENSP00000334346.6:p.Lys757=
ENST00000460137.6:c.2234A=	ENSP00000425003.1:p.Lys745=
ENST00000484238.6:n.1083A=
ENST00000508104.2:c.2270A=	ENSP00000426042.2:p.Lys757=
NM_001193376.1:c.2270A=	NP_001180305.1:p.Lys757=
NM_198253.2:c.2270A= , LRG_343t1:c.2270A=	NP_937983.2:p.Lys757=
XM_011514104.1:c.740A=	XP_011512406.1:p.Lys247=
XM_011514105.1:c.626A=	XP_011512407.1:p.Lys209=
XM_011514106.1:c.626A=	XP_011512408.1:p.Lys209=
NR_149162.1:n.2328A=
NR_149163.1:n.2292A=
NM_001193376.2:c.2270A=	NP_001180305.1:p.Lys757=
NM_198253.3:c.2270A= MANE Select	NP_937983.2:p.Lys757=
NR_149162.2:n.2349A=
NR_149163.2:n.2313A=
NM_001193376.3:c.2270A=	NP_001180305.1:p.Lys757=
NR_149162.3:n.2349A=
NR_149163.3:n.2313A=