Canonical Allele Identifier: CA1522564713
Gene: TERT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1278766G= , CM000667.2:g.1278766G= GRCh38
NC_000005.9:g.1278881G= , CM000667.1:g.1278881G= GRCh37
NC_000005.8:g.1331881G= NCBI36
NG_009265.1:g.21282C= , LRG_343:g.21282C=

Transcript Alleles

HGVS Amino-acid change
ENST00000310581.10:c.2161C= MANE Select ENSP00000309572.5:p.Pro721=
ENST00000656021.1:c.*1707C= ENSP00000499759.1:n.*1707C=
ENST00000310581.9:c.2161C= ENSP00000309572.5:p.Pro721=
ENST00000334602.10:c.2161C= ENSP00000334346.6:p.Pro721=
ENST00000460137.6:c.2131-6C= ENSP00000425003.1:n.2131-6C=
ENST00000484238.6:n.974C=
ENST00000508104.2:c.2161C= ENSP00000426042.2:p.Pro721=
NM_001193376.1:c.2161C= NP_001180305.1:p.Pro721=
NM_198253.2:c.2161C= , LRG_343t1:c.2161C= NP_937983.2:p.Pro721=
XM_011514104.1:c.631C= XP_011512406.1:p.Pro211=
XM_011514105.1:c.517C= XP_011512407.1:p.Pro173=
XM_011514106.1:c.517C= XP_011512408.1:p.Pro173=
NR_149162.1:n.2219C=
NR_149163.1:n.2189-6C=
NM_001193376.2:c.2161C= NP_001180305.1:p.Pro721=
NM_198253.3:c.2161C= MANE Select NP_937983.2:p.Pro721=
NR_149162.2:n.2240C=
NR_149163.2:n.2210-6C=
NM_001193376.3:c.2161C= NP_001180305.1:p.Pro721=
NR_149162.3:n.2240C=
NR_149163.3:n.2210-6C=