Canonical Allele Identifier: CA1522555304
Gene: TERT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1293570T= , CM000667.2:g.1293570T= GRCh38
NC_000005.9:g.1293685T= , CM000667.1:g.1293685T= GRCh37
NC_000005.8:g.1346685T= NCBI36
NG_009265.1:g.6478A= , LRG_343:g.6478A=

Transcript Alleles

HGVS Amino-acid change
ENST00000310581.10:c.1316A= MANE Select ENSP00000309572.5:p.Glu439=
ENST00000656021.1:c.1316A= ENSP00000499759.1:p.Glu439=
ENST00000310581.9:c.1316A= ENSP00000309572.5:p.Glu439=
ENST00000334602.10:c.1316A= ENSP00000334346.6:p.Glu439=
ENST00000460137.6:c.1316A= ENSP00000425003.1:p.Glu439=
ENST00000508104.2:c.1316A= ENSP00000426042.2:p.Glu439=
NM_001193376.1:c.1316A= NP_001180305.1:p.Glu439=
NM_198253.2:c.1316A= , LRG_343t1:c.1316A= NP_937983.2:p.Glu439=
NR_149162.1:n.1374A=
NR_149163.1:n.1374A=
NM_001193376.2:c.1316A= NP_001180305.1:p.Glu439=
NM_198253.3:c.1316A= MANE Select NP_937983.2:p.Glu439=
NR_149162.2:n.1395A=
NR_149163.2:n.1395A=
NM_001193376.3:c.1316A= NP_001180305.1:p.Glu439=
NR_149162.3:n.1395A=
NR_149163.3:n.1395A=