Canonical Allele Identifier: CA1522547868
Gene: TERT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1268492A= , CM000667.2:g.1268492A= GRCh38
NC_000005.9:g.1268607A= , CM000667.1:g.1268607A= GRCh37
NC_000005.8:g.1321607A= NCBI36
NG_009265.1:g.31556T= , LRG_343:g.31556T=

Transcript Alleles

HGVS Amino-acid change
ENST00000310581.10:c.2582+28T= MANE Select ENSP00000309572.5:n.2582+28T=
ENST00000656021.1:c.*2128+28T= ENSP00000499759.1:n.*2128+28T=
ENST00000310581.9:c.2582+28T= ENSP00000309572.5:n.2582+28T=
ENST00000334602.10:c.2582+28T= ENSP00000334346.6:n.2582+28T=
ENST00000460137.6:c.2364+28T= ENSP00000425003.1:n.2364+28T=
ENST00000484238.6:n.1213+28T=
ENST00000508104.2:c.2400+28T= ENSP00000426042.2:n.2400+28T=
NM_001193376.1:c.2582+28T= NP_001180305.1:n.2582+28T=
NM_198253.2:c.2582+28T= , LRG_343t1:c.2582+28T= NP_937983.2:n.2582+28T=
XM_011514104.1:c.1052+28T= XP_011512406.1:n.1052+28T=
XM_011514105.1:c.938+28T= XP_011512407.1:n.938+28T=
XM_011514106.1:c.938+28T= XP_011512408.1:n.938+28T=
NR_149162.1:n.2458+28T=
NR_149163.1:n.2422+28T=
NM_001193376.2:c.2582+28T= NP_001180305.1:n.2582+28T=
NM_198253.3:c.2582+28T= MANE Select NP_937983.2:n.2582+28T=
NR_149162.2:n.2479+28T=
NR_149163.2:n.2443+28T=
NM_001193376.3:c.2582+28T= NP_001180305.1:n.2582+28T=
NR_149162.3:n.2479+28T=
NR_149163.3:n.2443+28T=