Canonical Allele Identifier: CA2578275601
Gene: TERT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1272317_1272323del , CM000667.2:g.1272317_1272323del GRCh38
NC_000005.9:g.1272432_1272438del , CM000667.1:g.1272432_1272438del GRCh37
NC_000005.8:g.1325432_1325438del NCBI36
NG_009265.1:g.27725_27731del , LRG_343:g.27725_27731del

Transcript Alleles

HGVS Amino-acid Change
ENST00000310581.10:c.2287-43_2287-37del MANE Select ENSP00000309572.5:n.2287-43_2287-37del
ENST00000656021.1:c.*1833-43_*1833-37del ENSP00000499759.1:n.*1833-43_*1833-37del
ENST00000310581.9:c.2287-43_2287-37del ENSP00000309572.5:n.2287-43_2287-37del
ENST00000334602.10:c.2287-43_2287-37del ENSP00000334346.6:n.2287-43_2287-37del
ENST00000460137.6:c.2251-3690_2251-3684del ENSP00000425003.1:n.2251-3690_2251-3684del
ENST00000484238.6:n.1100-3690_1100-3684del
ENST00000508104.2:c.2287-3690_2287-3684del ENSP00000426042.2:n.2287-3690_2287-3684del
NM_001193376.1:c.2287-43_2287-37del NP_001180305.1:n.2287-43_2287-37del
NM_198253.2:c.2287-43_2287-37del , LRG_343t1:c.2287-43_2287-37del NP_937983.2:n.2287-43_2287-37del
XM_011514104.1:c.757-43_757-37del XP_011512406.1:n.757-43_757-37del
XM_011514105.1:c.643-43_643-37del XP_011512407.1:n.643-43_643-37del
XM_011514106.1:c.643-43_643-37del XP_011512408.1:n.643-43_643-37del
NR_149162.1:n.2345-3690_2345-3684del
NR_149163.1:n.2309-3690_2309-3684del
NM_001193376.2:c.2287-43_2287-37del NP_001180305.1:n.2287-43_2287-37del
NM_198253.3:c.2287-43_2287-37del MANE Select NP_937983.2:n.2287-43_2287-37del
NR_149162.2:n.2366-3690_2366-3684del
NR_149163.2:n.2330-3690_2330-3684del
NM_001193376.3:c.2287-43_2287-37del NP_001180305.1:n.2287-43_2287-37del
NR_149162.3:n.2366-3690_2366-3684del
NR_149163.3:n.2330-3690_2330-3684del