Canonical Allele Identifier: CA359079035
Gene: TERT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1278682T>C , CM000667.2:g.1278682T>C GRCh38
NC_000005.9:g.1278797T>C , CM000667.1:g.1278797T>C GRCh37
NC_000005.8:g.1331797T>C NCBI36
NG_009265.1:g.21366A>G , LRG_343:g.21366A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000310581.10:c.2245A>G MANE Select ENSP00000309572.5:p.Lys749Glu
ENST00000656021.1:c.*1791A>G ENSP00000499759.1:n.*1791A>G
ENST00000310581.9:c.2245A>G ENSP00000309572.5:p.Lys749Glu
ENST00000334602.10:c.2245A>G ENSP00000334346.6:p.Lys749Glu
ENST00000460137.6:c.2209A>G ENSP00000425003.1:p.Lys737Glu
ENST00000484238.6:n.1058A>G
ENST00000508104.2:c.2245A>G ENSP00000426042.2:p.Lys749Glu
NM_001193376.1:c.2245A>G NP_001180305.1:p.Lys749Glu
NM_198253.2:c.2245A>G , LRG_343t1:c.2245A>G NP_937983.2:p.Lys749Glu
XM_011514104.1:c.715A>G XP_011512406.1:p.Lys239Glu
XM_011514105.1:c.601A>G XP_011512407.1:p.Lys201Glu
XM_011514106.1:c.601A>G XP_011512408.1:p.Lys201Glu
NR_149162.1:n.2303A>G
NR_149163.1:n.2267A>G
NM_001193376.2:c.2245A>G NP_001180305.1:p.Lys749Glu
NM_198253.3:c.2245A>G MANE Select NP_937983.2:p.Lys749Glu
NR_149162.2:n.2324A>G
NR_149163.2:n.2288A>G
NM_001193376.3:c.2245A>G NP_001180305.1:p.Lys749Glu
NR_149162.3:n.2324A>G
NR_149163.3:n.2288A>G