Canonical Allele Identifier: CA359066780

Gene: TERT

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310581.10:c.3329C>G MANE Select	ENSP00000309572.5:p.Thr1110Arg
ENST00000656021.1:c.*2875C>G	ENSP00000499759.1:n.*2875C>G
ENST00000310581.9:c.3329C>G	ENSP00000309572.5:p.Thr1110Arg
ENST00000334602.10:c.3140C>G	ENSP00000334346.6:p.Thr1047Arg
ENST00000460137.6:c.2922C>G	ENSP00000425003.1:n.2922C>G
ENST00000484238.6:n.1771C>G
NM_001193376.1:c.3140C>G	NP_001180305.1:p.Thr1047Arg
NM_198253.2:c.3329C>G , LRG_343t1:c.3329C>G	NP_937983.2:p.Thr1110Arg
XM_011514104.1:c.1799C>G	XP_011512406.1:p.Thr600Arg
XM_011514105.1:c.1685C>G	XP_011512407.1:p.Thr562Arg
XM_011514106.1:c.1685C>G	XP_011512408.1:p.Thr562Arg
XR_925683.1:n.287-876G>C
NR_149162.1:n.3016C>G
NR_149163.1:n.2980C>G
NM_001193376.2:c.3140C>G	NP_001180305.1:p.Thr1047Arg
NM_198253.3:c.3329C>G MANE Select	NP_937983.2:p.Thr1110Arg
NR_149162.2:n.3037C>G
NR_149163.2:n.3001C>G
NM_001193376.3:c.3140C>G	NP_001180305.1:p.Thr1047Arg
NR_149162.3:n.3037C>G
NR_149163.3:n.3001C>G