Canonical Allele Identifier: CA1522558575
Gene: TERT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1272110A= , CM000667.2:g.1272110A= GRCh38
NC_000005.9:g.1272225A= , CM000667.1:g.1272225A= GRCh37
NC_000005.8:g.1325225A= NCBI36
NG_009265.1:g.27938T= , LRG_343:g.27938T=

Transcript Alleles

HGVS Amino-acid change
ENST00000310581.10:c.2382+75T= MANE Select ENSP00000309572.5:n.2382+75T=
ENST00000656021.1:c.*1928+75T= ENSP00000499759.1:n.*1928+75T=
ENST00000310581.9:c.2382+75T= ENSP00000309572.5:n.2382+75T=
ENST00000334602.10:c.2382+75T= ENSP00000334346.6:n.2382+75T=
ENST00000460137.6:c.2251-3477T= ENSP00000425003.1:n.2251-3477T=
ENST00000484238.6:n.1100-3477T=
ENST00000508104.2:c.2287-3477T= ENSP00000426042.2:n.2287-3477T=
NM_001193376.1:c.2382+75T= NP_001180305.1:n.2382+75T=
NM_198253.2:c.2382+75T= , LRG_343t1:c.2382+75T= NP_937983.2:n.2382+75T=
XM_011514104.1:c.852+75T= XP_011512406.1:n.852+75T=
XM_011514105.1:c.738+75T= XP_011512407.1:n.738+75T=
XM_011514106.1:c.738+75T= XP_011512408.1:n.738+75T=
NR_149162.1:n.2345-3477T=
NR_149163.1:n.2309-3477T=
NM_001193376.2:c.2382+75T= NP_001180305.1:n.2382+75T=
NM_198253.3:c.2382+75T= MANE Select NP_937983.2:n.2382+75T=
NR_149162.2:n.2366-3477T=
NR_149163.2:n.2330-3477T=
NM_001193376.3:c.2382+75T= NP_001180305.1:n.2382+75T=
NR_149162.3:n.2366-3477T=
NR_149163.3:n.2330-3477T=