Canonical Allele Identifier: CA359066783

Gene: TERT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1253798G>T , CM000667.2:g.1253798G>T	GRCh38
NC_000005.9:g.1253913G>T , CM000667.1:g.1253913G>T	GRCh37
NC_000005.8:g.1306913G>T	NCBI36
NG_009265.1:g.46250C>A , LRG_343:g.46250C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310581.10:c.3329C>A MANE Select	ENSP00000309572.5:p.Thr1110Lys
ENST00000656021.1:c.*2875C>A	ENSP00000499759.1:n.*2875C>A
ENST00000310581.9:c.3329C>A	ENSP00000309572.5:p.Thr1110Lys
ENST00000334602.10:c.3140C>A	ENSP00000334346.6:p.Thr1047Lys
ENST00000460137.6:c.2922C>A	ENSP00000425003.1:n.2922C>A
ENST00000484238.6:n.1771C>A
NM_001193376.1:c.3140C>A	NP_001180305.1:p.Thr1047Lys
NM_198253.2:c.3329C>A , LRG_343t1:c.3329C>A	NP_937983.2:p.Thr1110Lys
XM_011514104.1:c.1799C>A	XP_011512406.1:p.Thr600Lys
XM_011514105.1:c.1685C>A	XP_011512407.1:p.Thr562Lys
XM_011514106.1:c.1685C>A	XP_011512408.1:p.Thr562Lys
XR_925683.1:n.287-876G>T
NR_149162.1:n.3016C>A
NR_149163.1:n.2980C>A
NM_001193376.2:c.3140C>A	NP_001180305.1:p.Thr1047Lys
NM_198253.3:c.3329C>A MANE Select	NP_937983.2:p.Thr1110Lys
NR_149162.2:n.3037C>A
NR_149163.2:n.3001C>A
NM_001193376.3:c.3140C>A	NP_001180305.1:p.Thr1047Lys
NR_149162.3:n.3037C>A
NR_149163.3:n.3001C>A