Canonical Allele Identifier: CA1522558588
Gene: TERT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1272126C= , CM000667.2:g.1272126C= GRCh38
NC_000005.9:g.1272241C= , CM000667.1:g.1272241C= GRCh37
NC_000005.8:g.1325241C= NCBI36
NG_009265.1:g.27922G= , LRG_343:g.27922G=

Transcript Alleles

HGVS Amino-acid change
ENST00000310581.10:c.2382+59G= MANE Select ENSP00000309572.5:n.2382+59G=
ENST00000656021.1:c.*1928+59G= ENSP00000499759.1:n.*1928+59G=
ENST00000310581.9:c.2382+59G= ENSP00000309572.5:n.2382+59G=
ENST00000334602.10:c.2382+59G= ENSP00000334346.6:n.2382+59G=
ENST00000460137.6:c.2251-3493G= ENSP00000425003.1:n.2251-3493G=
ENST00000484238.6:n.1100-3493G=
ENST00000508104.2:c.2287-3493G= ENSP00000426042.2:n.2287-3493G=
NM_001193376.1:c.2382+59G= NP_001180305.1:n.2382+59G=
NM_198253.2:c.2382+59G= , LRG_343t1:c.2382+59G= NP_937983.2:n.2382+59G=
XM_011514104.1:c.852+59G= XP_011512406.1:n.852+59G=
XM_011514105.1:c.738+59G= XP_011512407.1:n.738+59G=
XM_011514106.1:c.738+59G= XP_011512408.1:n.738+59G=
NR_149162.1:n.2345-3493G=
NR_149163.1:n.2309-3493G=
NM_001193376.2:c.2382+59G= NP_001180305.1:n.2382+59G=
NM_198253.3:c.2382+59G= MANE Select NP_937983.2:n.2382+59G=
NR_149162.2:n.2366-3493G=
NR_149163.2:n.2330-3493G=
NM_001193376.3:c.2382+59G= NP_001180305.1:n.2382+59G=
NR_149162.3:n.2366-3493G=
NR_149163.3:n.2330-3493G=