Canonical Allele Identifier: CA1522564474
Gene: TERT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1278671A= , CM000667.2:g.1278671A= GRCh38
NC_000005.9:g.1278786A= , CM000667.1:g.1278786A= GRCh37
NC_000005.8:g.1331786A= NCBI36
NG_009265.1:g.21377T= , LRG_343:g.21377T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000310581.10:c.2256T= MANE Select ENSP00000309572.5:p.His752=
ENST00000656021.1:c.*1802T= ENSP00000499759.1:n.*1802T=
ENST00000310581.9:c.2256T= ENSP00000309572.5:p.His752=
ENST00000334602.10:c.2256T= ENSP00000334346.6:p.His752=
ENST00000460137.6:c.2220T= ENSP00000425003.1:p.His740=
ENST00000484238.6:n.1069T=
ENST00000508104.2:c.2256T= ENSP00000426042.2:p.His752=
NM_001193376.1:c.2256T= NP_001180305.1:p.His752=
NM_198253.2:c.2256T= , LRG_343t1:c.2256T= NP_937983.2:p.His752=
XM_011514104.1:c.726T= XP_011512406.1:p.His242=
XM_011514105.1:c.612T= XP_011512407.1:p.His204=
XM_011514106.1:c.612T= XP_011512408.1:p.His204=
NR_149162.1:n.2314T=
NR_149163.1:n.2278T=
NM_001193376.2:c.2256T= NP_001180305.1:p.His752=
NM_198253.3:c.2256T= MANE Select NP_937983.2:p.His752=
NR_149162.2:n.2335T=
NR_149163.2:n.2299T=
NM_001193376.3:c.2256T= NP_001180305.1:p.His752=
NR_149162.3:n.2335T=
NR_149163.3:n.2299T=