Canonical Allele Identifier: CA1072495769
Gene: TERT HGNC NCBI

Linked Data

dbSNP Id: rs1748125619

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1260219_1260220dup , CM000667.2:g.1260219_1260220dup GRCh38
NC_000005.9:g.1260334_1260335dup , CM000667.1:g.1260334_1260335dup GRCh37
NC_000005.8:g.1313334_1313335dup NCBI36
NG_009265.1:g.39829_39830dup , LRG_343:g.39829_39830dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000310581.10:c.2970+255_2970+256dup MANE Select ENSP00000309572.5:n.2970+255_2970+256dup
ENST00000656021.1:c.*2516+255_*2516+256dup ENSP00000499759.1:n.*2516+255_*2516+256dup
ENST00000667927.1:n.258+255_258+256dup
ENST00000310581.9:c.2970+255_2970+256dup ENSP00000309572.5:n.2970+255_2970+256dup
ENST00000334602.10:c.2781+255_2781+256dup ENSP00000334346.6:n.2781+255_2781+256dup
ENST00000460137.6:c.2563+255_2563+256dup ENSP00000425003.1:n.2563+255_2563+256dup
ENST00000484238.6:n.1412+255_1412+256dup
NM_001193376.1:c.2781+255_2781+256dup NP_001180305.1:n.2781+255_2781+256dup
NM_198253.2:c.2970+255_2970+256dup , LRG_343t1:c.2970+255_2970+256dup NP_937983.2:n.2970+255_2970+256dup
XM_011514104.1:c.1440+255_1440+256dup XP_011512406.1:n.1440+255_1440+256dup
XM_011514105.1:c.1326+255_1326+256dup XP_011512407.1:n.1326+255_1326+256dup
XM_011514106.1:c.1326+255_1326+256dup XP_011512408.1:n.1326+255_1326+256dup
NR_149162.1:n.2657+255_2657+256dup
NR_149163.1:n.2621+255_2621+256dup
NM_001193376.2:c.2781+255_2781+256dup NP_001180305.1:n.2781+255_2781+256dup
NM_198253.3:c.2970+255_2970+256dup MANE Select NP_937983.2:n.2970+255_2970+256dup
NR_149162.2:n.2678+255_2678+256dup
NR_149163.2:n.2642+255_2642+256dup
NM_001193376.3:c.2781+255_2781+256dup NP_001180305.1:n.2781+255_2781+256dup
NR_149162.3:n.2678+255_2678+256dup
NR_149163.3:n.2642+255_2642+256dup