Canonical Allele Identifier: CA359073187

Gene: TERT

Linked Data

• MyVariant Identifiers: chr5:g.1266606T>C (hg19) ; chr5:g.1266491T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1266491T>C , CM000667.2:g.1266491T>C	GRCh38
NC_000005.9:g.1266606T>C , CM000667.1:g.1266606T>C	GRCh37
NC_000005.8:g.1319606T>C	NCBI36
NG_009265.1:g.33557A>G , LRG_343:g.33557A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310581.10:c.2627A>G MANE Select	ENSP00000309572.5:p.His876Arg
ENST00000656021.1:c.*2173A>G	ENSP00000499759.1:n.*2173A>G
ENST00000310581.9:c.2627A>G	ENSP00000309572.5:p.His876Arg
ENST00000334602.10:c.2627A>G	ENSP00000334346.6:p.His876Arg
ENST00000460137.6:c.2409A>G	ENSP00000425003.1:n.2409A>G
ENST00000484238.6:n.1258A>G
ENST00000503656.1:n.34A>G
ENST00000508104.2:c.2445A>G	ENSP00000426042.2:n.2445A>G
NM_001193376.1:c.2627A>G	NP_001180305.1:p.His876Arg
NM_198253.2:c.2627A>G , LRG_343t1:c.2627A>G	NP_937983.2:p.His876Arg
XM_011514104.1:c.1097A>G	XP_011512406.1:p.His366Arg
XM_011514105.1:c.983A>G	XP_011512407.1:p.His328Arg
XM_011514106.1:c.983A>G	XP_011512408.1:p.His328Arg
NR_149162.1:n.2503A>G
NR_149163.1:n.2467A>G
NM_001193376.2:c.2627A>G	NP_001180305.1:p.His876Arg
NM_198253.3:c.2627A>G MANE Select	NP_937983.2:p.His876Arg
NR_149162.2:n.2524A>G
NR_149163.2:n.2488A>G
NM_001193376.3:c.2627A>G	NP_001180305.1:p.His876Arg
NR_149162.3:n.2524A>G
NR_149163.3:n.2488A>G