Canonical Allele Identifier: CA1522539837
Gene: TERT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1260522G= , CM000667.2:g.1260522G= GRCh38
NC_000005.9:g.1260637G= , CM000667.1:g.1260637G= GRCh37
NC_000005.8:g.1313637G= NCBI36
NG_009265.1:g.39526C= , LRG_343:g.39526C=

Transcript Alleles

HGVS Amino-acid change
ENST00000310581.10:c.2922C= MANE Select ENSP00000309572.5:p.Leu974=
ENST00000656021.1:c.*2468C= ENSP00000499759.1:n.*2468C=
ENST00000667927.1:n.210C=
ENST00000310581.9:c.2922C= ENSP00000309572.5:p.Leu974=
ENST00000334602.10:c.2733C= ENSP00000334346.6:p.Leu911=
ENST00000460137.6:c.2515C= ENSP00000425003.1:n.2515C=
ENST00000484238.6:n.1364C=
NM_001193376.1:c.2733C= NP_001180305.1:p.Leu911=
NM_198253.2:c.2922C= , LRG_343t1:c.2922C= NP_937983.2:p.Leu974=
XM_011514104.1:c.1392C= XP_011512406.1:p.Leu464=
XM_011514105.1:c.1278C= XP_011512407.1:p.Leu426=
XM_011514106.1:c.1278C= XP_011512408.1:p.Leu426=
NR_149162.1:n.2609C=
NR_149163.1:n.2573C=
NM_001193376.2:c.2733C= NP_001180305.1:p.Leu911=
NM_198253.3:c.2922C= MANE Select NP_937983.2:p.Leu974=
NR_149162.2:n.2630C=
NR_149163.2:n.2594C=
NM_001193376.3:c.2733C= NP_001180305.1:p.Leu911=
NR_149162.3:n.2630C=
NR_149163.3:n.2594C=