Canonical Allele Identifier: CA3184519

Gene: TERT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1271155C>T , CM000667.2:g.1271155C>T	GRCh38
NC_000005.9:g.1271270C>T , CM000667.1:g.1271270C>T	GRCh37
NC_000005.8:g.1324270C>T	NCBI36
NG_009265.1:g.28893G>A , LRG_343:g.28893G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_198253.3:c.2432G>A MANE Select	NP_937983.2:p.Arg811His
ENST00000310581.10:c.2432G>A MANE Select	ENSP00000309572.5:p.Arg811His
NM_001193376.1:c.2432G>A	NP_001180305.1:p.Arg811His
NM_001193376.2:c.2432G>A	NP_001180305.1:p.Arg811His
NM_001193376.3:c.2432G>A	NP_001180305.1:p.Arg811His
NM_198253.2:c.2432G>A , LRG_343t1:c.2432G>A	NP_937983.2:p.Arg811His
NR_149162.1:n.2345-2522G>A
NR_149162.2:n.2366-2522G>A
NR_149162.3:n.2366-2522G>A
NR_149163.1:n.2309-2522G>A
NR_149163.2:n.2330-2522G>A
NR_149163.3:n.2330-2522G>A
ENST00000310581.9:c.2432G>A	ENSP00000309572.5:p.Arg811His
ENST00000334602.10:c.2432G>A	ENSP00000334346.6:p.Arg811His
ENST00000460137.6:c.2251-2522G>A	ENSP00000425003.1:n.2251-2522G>A
ENST00000484238.6:n.1100-2522G>A
ENST00000508104.2:c.2287-2522G>A	ENSP00000426042.2:n.2287-2522G>A
ENST00000656021.1:c.*1978G>A	ENSP00000499759.1:n.*1978G>A
XM_011514104.1:c.902G>A	XP_011512406.1:p.Arg301His
XM_011514105.1:c.788G>A	XP_011512407.1:p.Arg263His
XM_011514106.1:c.788G>A	XP_011512408.1:p.Arg263His