Canonical Allele Identifier: CA1522548019
Gene: TERT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1268565T= , CM000667.2:g.1268565T= GRCh38
NC_000005.9:g.1268680T= , CM000667.1:g.1268680T= GRCh37
NC_000005.8:g.1321680T= NCBI36
NG_009265.1:g.31483A= , LRG_343:g.31483A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000310581.10:c.2537A= MANE Select ENSP00000309572.5:p.Tyr846=
ENST00000656021.1:c.*2083A= ENSP00000499759.1:n.*2083A=
ENST00000310581.9:c.2537A= ENSP00000309572.5:p.Tyr846=
ENST00000334602.10:c.2537A= ENSP00000334346.6:p.Tyr846=
ENST00000460137.6:c.2319A= ENSP00000425003.1:p.Leu773=
ENST00000484238.6:n.1168A=
ENST00000508104.2:c.2355A= ENSP00000426042.2:p.Leu785=
NM_001193376.1:c.2537A= NP_001180305.1:p.Tyr846=
NM_198253.2:c.2537A= , LRG_343t1:c.2537A= NP_937983.2:p.Tyr846=
XM_011514104.1:c.1007A= XP_011512406.1:p.Tyr336=
XM_011514105.1:c.893A= XP_011512407.1:p.Tyr298=
XM_011514106.1:c.893A= XP_011512408.1:p.Tyr298=
NR_149162.1:n.2413A=
NR_149163.1:n.2377A=
NM_001193376.2:c.2537A= NP_001180305.1:p.Tyr846=
NM_198253.3:c.2537A= MANE Select NP_937983.2:p.Tyr846=
NR_149162.2:n.2434A=
NR_149163.2:n.2398A=
NM_001193376.3:c.2537A= NP_001180305.1:p.Tyr846=
NR_149162.3:n.2434A=
NR_149163.3:n.2398A=