Canonical Allele Identifier: CA1522539619
Gene: TERT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1260346G= , CM000667.2:g.1260346G= GRCh38
NC_000005.9:g.1260461G= , CM000667.1:g.1260461G= GRCh37
NC_000005.8:g.1313461G= NCBI36
NG_009265.1:g.39702C= , LRG_343:g.39702C=

Transcript Alleles

HGVS Amino-acid change
ENST00000310581.10:c.2970+128C= MANE Select ENSP00000309572.5:n.2970+128C=
ENST00000656021.1:c.*2516+128C= ENSP00000499759.1:n.*2516+128C=
ENST00000667927.1:n.258+128C=
ENST00000310581.9:c.2970+128C= ENSP00000309572.5:n.2970+128C=
ENST00000334602.10:c.2781+128C= ENSP00000334346.6:n.2781+128C=
ENST00000460137.6:c.2563+128C= ENSP00000425003.1:n.2563+128C=
ENST00000484238.6:n.1412+128C=
NM_001193376.1:c.2781+128C= NP_001180305.1:n.2781+128C=
NM_198253.2:c.2970+128C= , LRG_343t1:c.2970+128C= NP_937983.2:n.2970+128C=
XM_011514104.1:c.1440+128C= XP_011512406.1:n.1440+128C=
XM_011514105.1:c.1326+128C= XP_011512407.1:n.1326+128C=
XM_011514106.1:c.1326+128C= XP_011512408.1:n.1326+128C=
NR_149162.1:n.2657+128C=
NR_149163.1:n.2621+128C=
NM_001193376.2:c.2781+128C= NP_001180305.1:n.2781+128C=
NM_198253.3:c.2970+128C= MANE Select NP_937983.2:n.2970+128C=
NR_149162.2:n.2678+128C=
NR_149163.2:n.2642+128C=
NM_001193376.3:c.2781+128C= NP_001180305.1:n.2781+128C=
NR_149162.3:n.2678+128C=
NR_149163.3:n.2642+128C=