Canonical Allele Identifier: CA1522574589
Gene: TERT HGNC NCBI

Linked Data

dbSNP Id: rs1579586262

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1286278T>A , CM000667.2:g.1286278T>A GRCh38
NC_000005.9:g.1286393T>A , CM000667.1:g.1286393T>A GRCh37
NC_000005.8:g.1339393T>A NCBI36
NG_009265.1:g.13770A>T , LRG_343:g.13770A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000310581.10:c.1574-3654A>T MANE Select ENSP00000309572.5:n.1574-3654A>T
ENST00000656021.1:c.*1006A>T ENSP00000499759.1:n.*1006A>T
ENST00000310581.9:c.1574-3654A>T ENSP00000309572.5:n.1574-3654A>T
ENST00000334602.10:c.1574-3654A>T ENSP00000334346.6:n.1574-3654A>T
ENST00000460137.6:c.1574-3654A>T ENSP00000425003.1:n.1574-3654A>T
ENST00000508104.2:c.1574-3654A>T ENSP00000426042.2:n.1574-3654A>T
NM_001193376.1:c.1574-3654A>T NP_001180305.1:n.1574-3654A>T
NM_198253.2:c.1574-3654A>T , LRG_343t1:c.1574-3654A>T NP_937983.2:n.1574-3654A>T
XM_011514104.1:c.-71A>T XP_011512406.1:n.-71A>T
XM_011514105.1:c.-226A>T XP_011512407.1:n.-226A>T
NR_149162.1:n.1632-3654A>T
NR_149163.1:n.1632-3654A>T
NM_001193376.2:c.1574-3654A>T NP_001180305.1:n.1574-3654A>T
NM_198253.3:c.1574-3654A>T MANE Select NP_937983.2:n.1574-3654A>T
NR_149162.2:n.1653-3654A>T
NR_149163.2:n.1653-3654A>T
NM_001193376.3:c.1574-3654A>T NP_001180305.1:n.1574-3654A>T
NR_149162.3:n.1653-3654A>T
NR_149163.3:n.1653-3654A>T