Canonical Allele Identifier: CA3184353

Gene: TERT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1260592C>T , CM000667.2:g.1260592C>T	GRCh38
NC_000005.9:g.1260707C>T , CM000667.1:g.1260707C>T	GRCh37
NC_000005.8:g.1313707C>T	NCBI36
NG_009265.1:g.39456G>A , LRG_343:g.39456G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_198253.3:c.2852G>A MANE Select	NP_937983.2:p.Arg951Gln
ENST00000310581.10:c.2852G>A MANE Select	ENSP00000309572.5:p.Arg951Gln
NM_001193376.1:c.2663G>A	NP_001180305.1:p.Arg888Gln
NM_001193376.2:c.2663G>A	NP_001180305.1:p.Arg888Gln
NM_001193376.3:c.2663G>A	NP_001180305.1:p.Arg888Gln
NM_198253.2:c.2852G>A , LRG_343t1:c.2852G>A	NP_937983.2:p.Arg951Gln
NR_149162.1:n.2539G>A
NR_149162.2:n.2560G>A
NR_149162.3:n.2560G>A
NR_149163.1:n.2503G>A
NR_149163.2:n.2524G>A
NR_149163.3:n.2524G>A
ENST00000310581.9:c.2852G>A	ENSP00000309572.5:p.Arg951Gln
ENST00000334602.10:c.2663G>A	ENSP00000334346.6:p.Arg888Gln
ENST00000460137.6:c.2445G>A	ENSP00000425003.1:n.2445G>A
ENST00000484238.6:n.1294G>A
ENST00000656021.1:c.*2398G>A	ENSP00000499759.1:n.*2398G>A
ENST00000667927.1:n.140G>A
XM_011514104.1:c.1322G>A	XP_011512406.1:p.Arg441Gln
XM_011514105.1:c.1208G>A	XP_011512407.1:p.Arg403Gln
XM_011514106.1:c.1208G>A	XP_011512408.1:p.Arg403Gln