Canonical Allele Identifier: CA1522574242
Gene: TERT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1285988A= , CM000667.2:g.1285988A= GRCh38
NC_000005.9:g.1286103A= , CM000667.1:g.1286103A= GRCh37
NC_000005.8:g.1339103A= NCBI36
NG_009265.1:g.14060T= , LRG_343:g.14060T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000310581.10:c.1574-3364T= MANE Select ENSP00000309572.5:n.1574-3364T=
ENST00000656021.1:c.*1119+177T= ENSP00000499759.1:n.*1119+177T=
ENST00000310581.9:c.1574-3364T= ENSP00000309572.5:n.1574-3364T=
ENST00000334602.10:c.1574-3364T= ENSP00000334346.6:n.1574-3364T=
ENST00000460137.6:c.1574-3364T= ENSP00000425003.1:n.1574-3364T=
ENST00000508104.2:c.1574-3364T= ENSP00000426042.2:n.1574-3364T=
NM_001193376.1:c.1574-3364T= NP_001180305.1:n.1574-3364T=
NM_198253.2:c.1574-3364T= , LRG_343t1:c.1574-3364T= NP_937983.2:n.1574-3364T=
XM_011514104.1:c.43+177T= XP_011512406.1:n.43+177T=
XM_011514105.1:c.-72+136T= XP_011512407.1:n.-72+136T=
XM_011514106.1:c.-161T= XP_011512408.1:n.-161T=
NR_149162.1:n.1632-3364T=
NR_149163.1:n.1632-3364T=
NM_001193376.2:c.1574-3364T= NP_001180305.1:n.1574-3364T=
NM_198253.3:c.1574-3364T= MANE Select NP_937983.2:n.1574-3364T=
NR_149162.2:n.1653-3364T=
NR_149163.2:n.1653-3364T=
NM_001193376.3:c.1574-3364T= NP_001180305.1:n.1574-3364T=
NR_149162.3:n.1653-3364T=
NR_149163.3:n.1653-3364T=