Canonical Allele Identifier: CA1522574666
Gene: TERT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1286343C= , CM000667.2:g.1286343C= GRCh38
NC_000005.9:g.1286458C= , CM000667.1:g.1286458C= GRCh37
NC_000005.8:g.1339458C= NCBI36
NG_009265.1:g.13705G= , LRG_343:g.13705G=

Transcript Alleles

HGVS Amino-acid change
ENST00000310581.10:c.1574-3719G= MANE Select ENSP00000309572.5:n.1574-3719G=
ENST00000656021.1:c.*941G= ENSP00000499759.1:n.*941G=
ENST00000310581.9:c.1574-3719G= ENSP00000309572.5:n.1574-3719G=
ENST00000334602.10:c.1574-3719G= ENSP00000334346.6:n.1574-3719G=
ENST00000460137.6:c.1574-3719G= ENSP00000425003.1:n.1574-3719G=
ENST00000508104.2:c.1574-3719G= ENSP00000426042.2:n.1574-3719G=
NM_001193376.1:c.1574-3719G= NP_001180305.1:n.1574-3719G=
NM_198253.2:c.1574-3719G= , LRG_343t1:c.1574-3719G= NP_937983.2:n.1574-3719G=
XM_011514104.1:c.-136G= XP_011512406.1:n.-136G=
XM_011514105.1:c.-291G= XP_011512407.1:n.-291G=
NR_149162.1:n.1632-3719G=
NR_149163.1:n.1632-3719G=
NM_001193376.2:c.1574-3719G= NP_001180305.1:n.1574-3719G=
NM_198253.3:c.1574-3719G= MANE Select NP_937983.2:n.1574-3719G=
NR_149162.2:n.1653-3719G=
NR_149163.2:n.1653-3719G=
NM_001193376.3:c.1574-3719G= NP_001180305.1:n.1574-3719G=
NR_149162.3:n.1653-3719G=
NR_149163.3:n.1653-3719G=